Polyester compositions containing furandicarboxylic acid or an ester thereof and cyclohexanedimethanol

ABSTRACT

Described are polyesters comprising (a) a dicarboxylic acid component comprising 2,5-furandicarboxylic acid residues and optionally, aromatic dicarboxylic acid residues and/or aliphatic dicarboxylic acid residues, and (b) a glycol component comprising 1,4-cyclohexanedimethanol residues and residues of a modifying glycol. The polyesters may be manufactured into articles such as fibers, films, bottles, coatings, or sheets.

FIELD OF THE INVENTION

The present invention generally relates to polyester compositions madefrom 2,5-furandicarboxylic acid or an ester thereof or mixtures thereof,and 1,4-cyclohexanedimethanol.

BACKGROUND OF THE INVENTION

Homopolymers based on 2,5-furandicarboxylic acid or an ester thereof and1,4-cyclohexanedimethanol are known in the art.

SUMMARY OF THE INVENTION

It is believed that certain copolyester compositions made from2,5-furandicarboxylic acid, an ester thereof, or mixtures thereof, and1,4-cyclohexanedimethanol are superior to polyesters known in the artwith respect to stable glass transition temperatures. Good barrierproperties have also been observed.

It is generally known that the more cyclohexanedimethanol that is addedto a polyester containing terephthalic acid, the greater its glasstransition temperature.

In certain embodiments of this invention, it has been surprisingly foundthat the more that cyclohexanedimethanol is added to a polyestercontaining 2,5-furandicarboxylic acid, the glass transition temperatureremains stable.

In one aspect, the invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of 2,5-furandicarboxylic acid and/or an        ester thereof;    -   ii) 0 to 30 mole % of other aromatic dicarboxylic acid residues        having up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 0.01 to 99 mole % of 1,4-cyclohexanedimethanol residues, and    -   ii) 1 to 99.99 mole % of residues of at least one modifying        glycol;        wherein the total mole % of the dicarboxylic acid component is        100 mole %, and the total mole % of the glycol component is 100        mole %.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of        2,2,4,4-tetramethyl-1,3-cyclobutanediol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.10 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 80 mole % of residues of        2,2,4,4-tetramethyl-1,3-cyclobutanediol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.10 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 80 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.10 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 80 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.10 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 80 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 65 to 75 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 25 to 35 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.35 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and wherein the glasstransition temperature is from 50° C. to 150° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 70 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 30 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 30 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 1 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 99 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 50 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 50 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 50 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 70 to 80 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 20 to 30 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 55 to 70 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 30 to 45 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 60 to 85 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 15 to 40 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 85 to 99 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 1 to 15 mole % of residues of at least one modifying glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 20 to 50 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 50 to 80 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 25 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 75 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one aspect, this invention relates to a polyester compositioncomprising at least one polyester which comprises:

(a) a dicarboxylic acid component comprising:

-   -   i) 80 to 100 mole % of residues of furandicarboxylic acid and/or        an ester thereof;    -   ii) 0 to 20 mole % of aromatic dicarboxylic acid residues having        up to 20 carbon atoms; and    -   iii) 0 to 20 mole % of aliphatic dicarboxylic acid residues        having up to 16 carbon atoms; and

(b) a glycol component comprising:

-   -   i) 30 to 35 mole % of 1,4-cyclohexanedimethanol residues; and    -   ii) 65 to 70 mole % of residues of at least one modifying        glycol,

wherein the total mole % of the dicarboxylic acid component is 100 mole%, and the total mole % of the glycol component is 100 mole %;

wherein the inherent viscosity of said polyester is from 0.50 to 1.2dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.; and

wherein the glass transition temperature is from 70° C. to 120° C.

In one embodiment, ethylene glycol can be a modifying glycol. In oneembodiment, ethylene glycol can be a modifying glycol. In oneembodiment, ethylene glycol can be the only modifying glycol. In oneembodiment, 2,2,4,4-tetramethyl-1,3-cyclobutanediol can be a modifyingglycol. In one embodiment, 2,2,4,4-tetramethyl-1,3-cyclobutanediol canbe the only modifying glycol. In one embodiment,2,2,4,4-tetramethyl-1,3-cyclobutanediol and ethylene glycol can bepresent as the modifying glycols.

In one embodiment, diethylene glycol may be present as an additionalmodifying glycol. Even if diethylene glycol is not specifically added,it is understood that diethylene glycol may be formed in situ and may bepresent in an embodiment where ethylene glycol is added as one of themonomers in the process of making the polyester. Even if diethyleneglycol is not specifically added, it is also understood that diethyleneglycol may be formed in situ and may be present in a minor amount suchas less than 2-3 mole %. Certain embodiments of polyesters of theinvention which are stated herein to not include additional modifyingglycols may or may not contain minor amounts of diethylene glycolresidues.

In any of the embodiments of the invention, the polyesters of theinvention comprise 2,5-furandicarboxylic acid (FDCA) can optionallycontain residues of terephthalic acid (TPA) and/or an ester thereof.Additional modifying dicarboxylic acid (or corresponding ester) residues(acids other than FDCA and TPA) can optionally be present.

In one embodiment, the polyesters of the invention can be used tomanufacture articles including, but not limited to, injection moldedarticles, injection blow molded articles, injection stretch blow moldedarticles, extrusion blow molded articles, extrusion stretch blow moldedarticles, extrusion coatings, calendered articles, compression moldedarticles, and solution casted articles.

In one embodiment, the polyesters of the invention can be used tomanufacture films, injection molded products, extrusion coatings,fibres, foams, thermoformed products, extruded profiles and sheets,extrusion blow molded articles, injection blow molded articles,rotomolded articles, stretch blow molded articles, etc.

Methods of making the articles of manufacuture, include, but are notlimited to, extrusion blow molding, extrusion stretch blow molding,injection blow molding, injection stretch blow molding, calendering,rotomolding, compression molding, and solution casting.

In another embodiment, the invention further relates to articles ofmanufacture comprising the film(s) and/or sheet(s) containing polyestercompositions described herein. In another embodiment, the inventionrelates to fibers. In yet another embodiment, the invention relates tofoams and/or foamed articles. In another embodiment, this inventionrelates to thermoformed articles.

The methods of forming polyesters into film(s) and/or sheet(s) are wellknown in the art. Examples of film(s) and/or sheet(s) of the inventionincluding but not limited to extruded film(s) and/or sheet(s),calendered film(s) and/or sheet(s), compression molded film(s) and/orsheet(s), solution casted film(s) and/or sheet(s). Examples of film orsheet production technologies include film blowing, casting (includingsolution casting), coextrusion, extrusion, calendering, and compressionmolding.

This invention relates to copolyester compositions based on2,5-furandicarboxylic acid or an ester thereof and1,4-cyclohexanedimethanol which are believed to provide greaterstability with respect to glass transition temperature than would beexpected by one of ordinary skill in the art.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a graphical representation of Table 1 data and depicts glasstransition temperature vs. mole percent CHDM for TPA-based andFDCA-based copolyesters.

DETAILED DESCRIPTION OF THE INVENTION

The present invention may be understood more readily by reference to thefollowing detailed description of certain embodiments of the inventionand the working examples. In accordance with the purpose(s) of thisinvention, certain embodiments of the invention are described in theSummary of the Invention and are further described herein below. Also,other embodiments of the invention are described herein.

Copolyesters synthesized from 2,5-furandicarboxylic acid (FDCA) or itsderivatives with 1,4-cyclohexanedimethanol (CHDM) have an advantage ofnearly constant glass transition temperature (Tg) over a wide range ofcompositions, compared to commercial terephthalic acid-basedcopolyesters (PET, PETG, PCTG, PCT), for which Tg varies measurably ascomposition varies. This advantage may be beneficial for producingcopolyesters with constant Tg even if composition varies duringmanufacturing.

The term “polyester”, as used herein, is intended to include“copolyesters” and is understood to mean a synthetic polymer prepared bythe reaction of one or more difunctional carboxylic acids and/ormultifunctional carboxylic acids with one or more difunctional hydroxylcompounds and/or multifunctional hydroxyl compounds. Typically thedifunctional carboxylic acid can be a dicarboxylic acid and thedifunctional hydroxyl compound can be a dihydric alcohol such as, forexample, glycols and diols. The term “glycol” as used in thisapplication includes, but is not limited to, diols, glycols, and/ormultifunctional hydroxyl compounds, for example, branching agents.Alternatively, a difunctional carboxylic acid may be a hydroxycarboxylic acid such as, for example, p-hydroxybenzoic acid, and thedifunctional hydroxyl compound may be an aromatic nucleus bearing 2hydroxyl substituents such as, for example, hydroquinone. The term“residue”, as used herein, means any organic structure incorporated intoa polymer through a polycondensation and/or an esterification reactionfrom the corresponding monomer. The term “repeating unit”, as usedherein, means an organic structure having a dicarboxylic acid residueand a diol residue. Thus, for example, the dicarboxylic acid residuesmay be derived from a dicarboxylic acid monomer or its associated acidhalides, esters, salts, anhydrides, or mixtures thereof. As used herein,therefore, the term dicarboxylic acid is intended to includedicarboxylic acids and any derivative of a dicarboxylic acid, includingits associated acid halides, esters, half-esters, salts, half-salts,anhydrides, mixed anhydrides, or mixtures thereof, useful in a reactionprocess with a diol to make polyester. Furthermore, as used in thisapplication, the term “diacid” includes multifunctional acids, forexample, branching agents. As used herein, the term “terephthalic acid”is intended to include terephthalic acid itself and residues thereof aswell as any derivative of terephthalic acid, including its associatedacid halides, esters, half-esters, salts, half-salts, anhydrides, mixedanhydrides, or mixtures thereof or residues thereof useful in a reactionprocess with a diol to make polyester.

In one embodiment, furandicarboxylic acid and/or its ester may be usedas a starting material. In yet another embodiment, mixtures of2,5-furandicarboxylic acid and its ester may be used as the startingmaterial and/or as an intermediate material.

Terephthalic acid and/or its ester may also be used in one embodiment asone of the starting materials, with 2,5-furandicarboxylic acid and/orits ester. In another embodiment, dimethyl terephthalate may be usedinstead of terephthalic acid as a starting material. In yet anotherembodiment, mixtures of terephthalic acid and dimethyl terephthalate maybe used as starting materials and/or as an intermediate material.

Isophthalic acid and/or its ester may also be used in one embodiment asone of the starting materials, with 2,5-furandicarboxylic acid and/orits ester.

In another embodiment, terephthalic acid and/or its ester as well asisophthalic acid and/or its ester may also be used in combination asstarting materials, with 2,5-furandicarboxylic acid and/or its ester.

The polyesters used in the present invention typically can be preparedfrom dicarboxylic acids and diols which react in substantially equalproportions and are incorporated into the polyester polymer as theircorresponding residues. The polyesters of the present invention,therefore, can contain substantially equal molar proportions of acidresidues (100 mole %) and diol (and/or multifunctional hydroxylcompounds) residues (100 mole %) such that the total moles of repeatingunits is equal to 100 mole %. The mole percentages provided in thepresent disclosure, therefore, may be based on the total moles of acidresidues, the total moles of diol residues, or the total moles ofrepeating units. For example, a polyester containing 30 mole %isophthalic acid, based on the total acid residues, means the polyestercontains 30 mole % isophthalic acid residues out of a total of 100 mole% acid residues. Thus, there are 30 moles of isophthalic acid residuesamong every 100 moles of acid residues. In another example, a polyestercontaining 30 mole % 1,4-cyclohexanedimethanol, based on the total diolresidues, means the polyester contains 30 mole 1,4-cyclohexanedimethanolresidues out of a total of 100 mole % diol residues. Thus, there are 30moles of 1,4-cyclohexanedimethanol residues among every 100 moles ofdiol residues.

In other aspects of the invention, the Tg of the polyesters useful inthe invention can be at least one of the following ranges: 30 to 130°C.; 30 to 125° C.; 30 to 120° C.; 30 to 115° C.; 30 to 110° C.; 30 to105° C.; 30 to 100° C.; 30 to 95° C.; 30 to 90° C.; 30 to 85° C.; 30 to80° C.; 30 to 75° C.; 30 to 70° C.; 30 to 65° C.; 30 to 60° C.; 30 to55° C.; 30 to 50° C.; 30 to 45° C.; 35 to 130° C.; 35 to 125° C.; 35 to120° C.; 35 to 115° C.; 35 to 110° C.; 35 to 105° C.; 35 to 100° C.; 35to 95° C.; 35 to 90° C.; 35 to 85° C.; 35 to 80° C.; 35 to 75° C.; 35 to70° C.; 35 to 65° C.; 35 to 60° C.; 35 to 55° C.; 35 to 50° C.; 35 to45° C.; 40 to 130° C.; 40 to 125° C.; 40 to 120° C.; 40 to 115° C.; 40to 110° C.; 40 to 105° C.; 40 to 100° C.; 40 to 95° C.; 40 to 90° C.; 40to 85° C.; 40 to 80° C.; 40 to 75° C.; 40 to 70° C.; 40 to 65° C.; 40 to60° C.; 40 to 55° C.; 45 to 130° C.; 45 to 125° C.; 45 to 120° C.; 45 to115° C.; 45 to 110° C.; 45 to 105° C.; 45 to 100° C.; 45 to 95° C.; 45to 90° C.; 45 to 85° C.; 45 to 80° C.; 45 to 75° C.; 45 to 70° C.; 45 to65° C.; 45 to 60° C.; 45 to 55° C.; 50 to 130° C.; 50 to 125° C.; 50 to120° C.; 50 to 115° C.; 50 to 110° C.; 50 to 105° C.; 50 to 100° C.; 50to 95° C.; 50 to 90° C.; 50 to 85° C.; 50 to 80° C.; 50 to 75° C.; 50 to70° C.; 50 to 65° C.; 55 to 130° C.; 55 to 125° C.; 55 to 120° C.; 55 to115° C.; 55 to 110° C.; 55 to 105° C.; 55 to 100° C.; 55 to 95° C.; 55to 90° C.; 55 to 85° C.; 55 to 80° C.; 55 to 75° C.; 55 to 70° C.; 55 to65° C.; 60 to 130° C.; 60 to 125° C.; 60 to 120° C.; 60 to 115° C.; 60to 110° C.; 60 to 105° C.; 60 to 100° C.; 60 to 95° C.; 60 to 90° C.; 60to 85° C.; 60 to 80° C.; 60 to 75° C.; 60 to 70° C.; 65 to 130° C.; 65to 125° C.; 65 to 120° C.; 65 to 115° C.; 65 to 110° C.; 65 to 105° C.;65 to 100° C.; 65 to 95° C.; 65 to 90° C.; 65 to 85° C.; 65 to 80° C.;65 to 75° C.; 65 to 70° C.; 70 to 130° C.; 70 to 125° C.; 70 to 120° C.;70 to 115° C.; 70 to 110° C.; 70 to 105° C.; 70 to 100° C.; 70 to 95°C.; 70 to 90° C.; 70 to 85° C.; 70 to 80° C.; 70 to 75° C.; 75 to 130°C.; 75 to 125° C.; 75 to 120° C.; 75 to 115° C.; 75 to 110° C.; 75 to105° C.; 75 to 100° C.; 75 to 95° C.; 75 to 90° C.; 75 to 85° C.; 75 to80° C.; 80 to 130° C.; 80 to 125° C.; 80 to 120° C.; 80 to 115° C.; 80to 110° C.; 80 to 105° C.; 80 to 100° C.; 80 to 95° C.; 80 to 90° C.; 85to 130° C.; 85 to 125° C.; 85 to 120° C.; 85 to 115° C.; 85 to 110° C.;85 to 105° C.; 85 to 100° C.; 85 to 95° C.; 85 to 90° C.; 90 to 130° C.;90 to 125° C.; 90 to 120° C.; 90 to 115° C.; 90 to 110° C.; 90 to 105°C.; 90 to 100° C.; 90 to 95° C.; 95 to 130° C.; 95 to 125° C.; 95 to120° C.; 95 to 115° C.; 95 to 110° C.; 95 to 105° C.; 95 to 100° C.; 100to 130° C.; 100 to 125° C.; 100 to 120° C.; 100 to 115° C.; or 100 to110° C.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 99 mole %1,4-cyclohexanedimethanol and 1 to 99.99 mole % of at least onemodifying glycol; 1 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 99mole % of at least one modifying glycol; 5 to 99 mole %1,4-cyclohexanedimethanol and 1 to 95 mole % at least one modifyingglycol; 10 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 90 mole % ofat least one modifying glycol; 15 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 85 mole % of at least one modifying glycol; 20 to 99 mole %1,4-cyclohexanedimethanol and 1 to 80 mole % of at least one modifyingglycol; 25 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 75 mole % ofat least one modifying glycol; 30 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 70 mole % of at least one modifying glycol; 35 to 99 mole %1,4-cyclohexanedimethanol and 1 to 65 mole % of at least one modifyingglycol; 40 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 60 mole % ofat least one modifying glycol; 45 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 55 mole % of at least one modifying glycol; 50 to 99 mole %1,4-cyclohexanedimethanol and 1 to 50 mole % of at least one modifyingglycol; 55 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 45 mole % ofat least one modifying glycol; 60 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 40 mole % of at least one modifying glycol; 65 to 99 mole %1,4-cyclohexanedimethanol and 1 to 35 mole % of at least one modifyingglycol; 70 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 30 mole % ofat least one modifying glycol; 75 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 25 mole % of at least one modifying glycol; 80 to 99 mole %1,4-cyclohexanedimethanol and 1 to 20 mole % of at least one modifyingglycol; 85 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 15 mole % ofat least one modifying glycol; 90 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 10 mole % of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 95 mole %1,4-cyclohexanedimethanol and 5 to 99.99 mole % of at least onemodifying glycol; 1 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 99mole % of at least one modifying glycol; 5 to 95 mole %1,4-cyclohexanedimethanol and 5 to 95 mole % of at least one modifyingglycol; 10 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 90 mole % ofat least one modifying glycol; 15 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 85 mole % of at least one modifying glycol; 20 to 95 mole %1,4-cyclohexanedimethanol and 5 to 80 mole % of at least one modifyingglycol; 25 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 75 mole % ofat least one modifying glycol; 30 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 70 mole % of at least one modifying glycol; 35 to 95 mole %1,4-cyclohexanedimethanol and 5 to 65 mole % of at least one modifyingglycol; 40 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 60 mole % ofat least one modifying glycol; 45 to 95 mole % 1,4-cyclohexanedimethanoland 6 to 55 mole % of at least one modifying glycol; 50 to 95 mole %1,4-cyclohexanedimethanol and 5 to 50 mole % of at least one modifyingglycol; 55 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 45 mole % ofat least one modifying glycol; 60 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 40 mole % of at least one modifying glycol; 65 to 95 mole %1,4-cyclohexanedimethanol and 5 to 35 mole % of at least one modifyingglycol; 70 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 30 mole % ofat least one modifying glycol; 75 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 25 mole % of at least one modifying glycol; 80 to 95 mole %1,4-cyclohexanedimethanol and 5 to 20 mole % of at least one modifyingglycol; 85 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 15 mole % ofat least one modifying glycol; 90 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 10 mole % of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 90 mole %1,4-cyclohexanedimethanol and 10 to 99.99 mole % of at least onemodifying glycol; 1 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 99mole % of at least one modifying glycol; 5 to 90 mole %1,4-cyclohexanedimethanol and 10 to 95 mole % of at least one modifyingglycol; 10 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 90 mole % ofat least one modifying glycol; 15 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 85 mole % of at least one modifying glycol; 20 to 90 mole %1,4-cyclohexanedimethanol and 10 to 80 mole % of at least one modifyingglycol, 25 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 75 mole % ofat least one modifying glycol; 30 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 70 mole % of at least one modifying glycol; 35 to 90 mole %1,4-cyclohexanedimethanol and 10 to 65 mole % of at least one modifyingglycol; 40 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 60 mole % ofat least one modifying glycol; 45 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 55 mole % of at least one modifying glycol; 50 to 90 mole %1,4-cyclohexanedimethanol and 10 to 50 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 90 mole %1,4-cyclohexanedimethanol and 10 to 45 mole % of at least one modifyingglycol; 60 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 40 mole % ofat least one modifying glycol; 65 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 35 mole % of at least one modifying glycol; 70 to 90 mole %1,4-cyclohexanedimethanol and 10 to 30 mole % of at least one modifyingglycol; 75 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 25 mole % ofat least one modifying glycol; 80 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 20 mole % of at least one modifying glycol; 85 to 90 mole %1,4-cyclohexanedimethanol and 10 to 15 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 85 mole %1,4-cyclohexanedimethanol and 15 to 99.99 mole % of at least onemodifying glycol; 1 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 99mole % of at least one modifying glycol; 5 to 85 mole %1,4-cyclohexanedimethanol and 15 to 95 mole % of at least one modifyingglycol; 10 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 90 mole % ofat least one modifying glycol; 15 to 85 mole % 1,4-cyclohexanedimethanoland 15 to 85 mole % of at least one modifying glycol; 20 to 85 mole %1,4-cyclohexanedimethanol and 15 to 80 mole % of at least one modifyingglycol; 25 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 75 mole % ofat least one modifying glycol; 30 to 85 mole % 1,4-cyclohexanedimethanoland 15 to 70 mole % of at least one modifying glycol; 35 to 85 mole %1,4-cyclohexanedimethanol and 15 to 65 mole % of at least one modifyingglycol; 40 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 60 mole % ofat least one modifying glycol; 45 to 85 mole % 1,4-cyclohexanedimethanol15 to 55 mole % of at least one modifying glycol; 50 to 85 mole %1,4-cyclohexanedimethanol and 15 to 50 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 85 mole %1,4-cyclohexanedimethanol and 15 to 45 mole % of at least one modifyingglycol; 60 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 40 mole % ofat least one modifying glycol; 65 to 85 mole % 1,4-cyclohexanedimethanoland 15 to 35 mole % of at least one modifying glycol; 70 to 85 mole %1,4-cyclohexanedimethanol and 15 to 30 mole % of at least one modifyingglycol; 75 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 25 mole % ofat least one modifying glycol; 80 to 85 mole % 1,4-cyclohexanedimethanoland 15 to 20 mole % of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 80 mole %1,4-cyclohexanedimethanol and 20 to 99.99 mole % of at least onemodifying glycol; 1 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 99mole % of at least one modifying glycol; 5 to 80 mole %1,4-cyclohexanedimethanol and 20 to 95 mole % of at least one modifyingglycol; 10 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 90 mole % ofat least one modifying glycol; 15 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 85 mole % of at least one modifying glycol; 20 to 80 mole %1,4-cyclohexanedimethanol and 20 to 80 mole % of at least one modifyingglycol; 25 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 75 mole % ofat least one modifying glycol; 30 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 70 mole % of at least one modifying glycol; 35 to 80 mole %1,4-cyclohexanedimethanol and 20 to 65 mole % of at least one modifyingglycol; 40 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 60 mole % ofat least one modifying glycol; 45 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 55 mole % of at least one modifying glycol; 50 to 80 mole %1,4-cyclohexanedimethanol and 20 to 50 mole % of at least one modifyingglycol; 55 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 45 mole % ofat least one modifying glycol; 60 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 40 mole % of at least one modifying glycol; 65 to 80 mole %1,4-cyclohexanedimethanol and 20 to 35 mole % of at least one modifyingglycol; 70 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 30 mole % ofat least one modifying glycol; and 75 to 80 mole %1,4-cyclohexanedimethanol and 20 to 25 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 75 mole %1,4-cyclohexanedimethanol and 25 to 99.99 mole % of at least onemodifying glycol; 1 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 99mole % of at least one modifying glycol; to 75 mole %1,4-cyclohexanedimethanol and 25 to 95 mole % of at least one modifyingglycol; 10 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 90 mole % ofat least one modifying glycol; 15 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 85 mole % of at least one modifying glycol; 20 to 75 mole %1,4-cyclohexanedimethanol and 25 to 80 mole % of at least one modifyingglycol; 25 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 75 mole % ofat least one modifying glycol; 30 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 70 mole % of at least one modifying glycol; 35 to 75 mole %1,4-cyclohexanedimethanol and 25 to 65 mole % of at least one modifyingglycol; 40 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 60 mole % ofat least one modifying glycol; 45 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 55 mole % of at least one modifying glycol; 50 to 75 mole %1,4-cyclohexanedimethanol and 25 to 50 mole % of at least one modifyingglycol; 55 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 45 mole % ofat least one modifying glycol; 60 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 40 mole % of at least one modifying glycol; 65 to 75 mole %1,4-cyclohexanedimethanol and 25 to 35 mole % of at least one modifyingglycol; and 70 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 30 mole% of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 65 mole %1,4-cyclohexanedimethanol and 35 to 99.99 mole % of at least onemodifying glycol; 1 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 99mole % of at least one modifying glycol; 5 to 65 mole %1,4-cyclohexanedimethanol and 35 to 95 mole % of at least one modifyingglycol; 10 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 90 mole % ofat least one modifying glycol; 15 to 65 mole % 1,4-cyclohexanedimethanoland 35 to 85 mole % of at least one modifying glycol; 20 to 65 mole %1,4-cyclohexanedimethanol and 35 to 80 mole % of at least one modifyingglycol, 25 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 75 mole % ofat least one modifying glycol; 30 to 65 mole % 1,4-cyclohexanedimethanoland 35 to 70 mole % of at least one modifying glycol; 35 to 65 mole %1,4-cyclohexanedimethanol and 35 to 65 mole % of at least one modifyingglycol; 40 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 60 mole % ofat least one modifying glycol; 45 to 65 mole % 1,4-cyclohexanedimethanoland 35 to 55 mole % of at least one modifying glycol; 50 to 65 mole %1,4-cyclohexanedimethanol and 35 to 50 mole % of at least one modifyingglycol; 55 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 45 mole % ofat least one modifying glycol; and 60 to 65 mole %1,4-cyclohexanedimethanol and 35 to 40 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 60 mole %1,4-cyclohexanedimethanol and 40 to 99.99 mole % of at least onemodifying glycol; 1 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 99mole % of at least one modifying glycol; 5 to 60 mole %1,4-cyclohexanedimethanol and 40 to 95 mole % of at least one modifyingglycol; 10 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 90 mole % ofat least one modifying glycol; 15 to 60 mole % 1,4-cyclohexanedimethanoland 40 to 85 mole % of at least one modifying glycol; 20 to 60 mole %1,4-cyclohexanedimethanol and 40 to 80 mole % of at least one modifyingglycol; 25 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 75 mole % ofat least one modifying glycol; 30 to 60 mole % 1,4-cyclohexanedimethanoland 40 to 70 mole % of at least one modifying glycol; 35 to 60 mole %1,4-cyclohexanedimethanol and 40 to 65 mole % of at least one modifyingglycol; 40 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 60 mole % ofat least one modifying glycol; 45 to 60 mole % 1,4-cyclohexanedimethanoland 40 to 55 mole % of at least one modifying glycol; 50 to 60 mole %1,4-cyclohexanedimethanol and 40 to 50 mole % of at least one modifyingglycol; 55 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 45 mole % ofat least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 55 mole %1,4-cyclohexanedimethanol and 45 to 99.99 mole % of at least onemodifying glycol; 1 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 99mole % of at least one modifying glycol; 5 to 55 mole %1,4-cyclohexanedimethanol and 45 to 95 mole % of at least one modifyingglycol; 10 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 90 mole % ofat least one modifying glycol; 15 to 55 mole % 1,4-cyclohexanedimethanoland 45 to 85 mole % of at least one modifying glycol; 20 to 55 mole %1,4-cyclohexanedimethanol and 45 to 80 mole % of at least one modifyingglycol; 25 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 75 mole % ofat least one modifying glycol; 30 to 55 mole % 1,4-cyclohexanedimethanoland 45 to 70 mole % of at least one modifying glycol; 35 to 55 mole %1,4-cyclohexanedimethanol and 45 to 65 mole % of at least one modifyingglycol; 40 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 60 mole % ofat least one modifying glycol; 45 to 55 mole % 1,4-cyclohexanedimethanoland 45 to 55 mole % of at least one modifying glycol; and 50 to 55 mole% 1,4-cyclohexanedimethanol and 45 to 50 mole % of at least onemodifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 50 mole %1,4-cyclohexanedimethanol and 50 to 99.99 mole % of at least onemodifying glycol; 1 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 99mole % of at least one modifying glycol; 5 to 50 mole %1,4-cyclohexanedimethanol and 50 to 95 mole % of at least one modifyingglycol; 10 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 90 mole % ofat least one modifying glycol; 15 to 50 mole % 1,4-cyclohexanedimethanoland 50 to 85 mole % of at least one modifying glycol; 20 to 50 mole %1,4-cyclohexanedimethanol and 50 to 80 mole % of at least one modifyingglycol 25 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 75 mole % ofat least one modifying glycol; 30 to 50 mole % 1,4-cyclohexanedimethanoland 50 to 70 mole % of at least one modifying glycol; 35 to 50 mole %1,4-cyclohexanedimethanol and 50 to 65 mole % of at least one modifyingglycol; 40 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 60 mole % ofat least one modifying glycol; and 45 to 50 mole %1,4-cyclohexanedimethanol and 50 to 55 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 45 mole %1,4-cyclohexanedimethanol and 55 to 99.99 mole % of at least onemodifying glycol; 1 to 45 mole % 1,4-cyclohexanedimethanol and 55 to 99mole % of at least one modifying glycol; 5 to 45 mole %1,4-cyclohexanedimethanol and 50 to 95 mole % of at least one modifyingglycol; 10 to 45 and 55 to 95 mole % of at least one modifying glycolmole % 1,4-cyclohexanedimethanol; 15 to 45 mole %1,4-cyclohexanedimethanol and 55 to 85 mole % of at least one modifyingglycol; 20 to 45 mole % 1,4-cyclohexanedimethanol and 55 to 80 mole % ofat least one modifying glycol; 25 to 45 mole % 1,4-cyclohexanedimethanoland 55 to 75 mole % of at least one modifying glycol; 30 to 45 mole %1,4-cyclohexanedimethanol and 55 to 65 mole % of at least one modifyingglycol; 35 to 45 mole % 1,4-cyclohexanedimethanol and 55 to 65 mole % ofat least one modifying glycol; 40 to 45 mole % 1,4-cyclohexanedimethanoland 55 to 60 mole % of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 40 mole %1,4-cyclohexanedimethanol and 60 to 99.99 mole % of at least onemodifying glycol; 1 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 99mole % of at least one modifying glycol; 5 to 40 mole %1,4-cyclohexanedimethanol and 60 to 95 mole % of at least one modifyingglycol; 10 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 90 mole % ofat least one modifying glycol; 15 to 40 mole % 1,4-cyclohexanedimethanoland 60 to 85 mole % of at least one modifying glycol; 20 to 40 mole %1,4-cyclohexanedimethanol and 60 to 80 mole % of at least one modifyingglycol; 25 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 75 mole % ofat least one modifying glycol; 30 to 40 mole % 1,4-cyclohexanedimethanoland 60 to 70 mole % of at least one modifying glycol; 35 to 40 mole %1,4-cyclohexanedimethanol and 60 to 65 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 35 mole %1,4-cyclohexanedimethanol and 65 to 99.99 mole % of at least onemodifying glycol; 1 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 99mole % of at least one modifying glycol; 5 to 35 mole %1,4-cyclohexanedimethanol and 65 to 95 mole % of at least one modifyingglycol; 10 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 90 mole % ofat least one modifying glycol; 15 to 35 mole % 1,4-cyclohexanedimethanoland 65 to 85 mole % of at least one modifying glycol; 20 to 35 mole %1,4-cyclohexanedimethanol and 65 to 80 mole % of at least one modifyingglycol; 25 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 75 mole % ofat least one modifying glycol; 30 to 35 mole % 1,4-cyclohexanedimethanoland 65 to 70 mole % of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 30 mole %1,4-cyclohexanedimethanol and 70 to 99.99 mole % mole % of at least onemodifying glycol; 1 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 99mole % of at least one modifying glycol; 5 to 30 mole %1,4-cyclohexanedimethanol and 70 to 95 mole % of at least one modifyingglycol; 10 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 90 mole % ofat least one modifying glycol; 15 to 30 mole % 1,4-cyclohexanedimethanoland 70 to 85 mole % of at least one modifying glycol; 20 to 30 mole %1,4-cyclohexanedimethanol and 70 to 80 mole % of at least one modifyingglycol; 25 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 75 mole % ofat least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 25 mole %1,4-cyclohexanedimethanol and 75 to 99.99 mole % of at least onemodifying glycol; 1 to 25 mole % 1,4-cyclohexanedimethanol and 75 to 99mole % of at least one modifying glycol; 5 to 25 mole %1,4-cyclohexanedimethanol and 75 to 95 mole % of at least one modifyingglycol; 10 to 25 mole % 1,4-cyclohexanedimethanol and 75 to 90 mole % ofat least one modifying glycol; 15 to 25 mole % 1,4-cyclohexanedimethanoland 75 to 85 mole % of at least one modifying glycol; 20 to 25 mole %1,4-cyclohexanedimethanol and 75 to 80 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 20 mole %1,4-cyclohexanedimethanol and 80 to 99.99 mole % of at least onemodifying glycol; 1 to 20 mole % 1,4-cyclohexanedimethanol and 80 to 99mole % of at least one modifying glycol; 5 to 20 mole %1,4-cyclohexanedimethanol and 80 to 95 mole % of at least one modifyingglycol; 10 to 20 mole % 1,4-cyclohexanedimethanol and 80 to 90 mole % ofat least one modifying glycol; and 15 to 20 mole %1,4-cyclohexanedimethanol and 80 to 85 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 15 mole %1,4-cyclohexanedimethanol and 85 to 99.99 mole % of at least onemodifying glycol; 1 to 15 mole % 1,4-cyclohexanedimethanol and 85 to 99mole % of at least one modifying glycol; 5 to 15 mole %1,4-cyclohexanedimethanol and 85 to 95 mole % of at least one modifyingglycol; and 10 to 15 mole % 1,4-cyclohexanedimethanol and 85 to 90 mole% of at least one modifying glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 10 mole %1,4-cyclohexanedimethanol and 90 to 99.99 mole % of at least onemodifying glycol; 1 to 10 mole % 1,4-cyclohexanedimethanol and 90 to 99mole % of at least one modifying glycol; 5 to 10 mole %1,4-cyclohexanedimethanol and 90 to 95 mole % of at least one modifyingglycol; 0.01 to 5 mole % 1,4-cyclohexanedimethanol and 95 to 99.99 mole% of at least one modifying glycol and 1 to 5 mole %1,4-cyclohexanedimethanol and 95 to 99 mole % of at least one modifyingglycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 99 mole %1,4-cyclohexanedimethanol and 1 to 99.99 mole % ethylene glycol; 1 to 99mole % 1,4-cyclohexanedimethanol and 1 to 99 mole % ethylene glycol; 5to 99 mole % 1,4-cyclohexanedimethanol and 1 to 95 mole % ethyleneglycol; 10 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 90 mole %ethylene glycol; 15 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 85mole % ethylene glycol; 20 to 99 mole % 1,4-cyclohexanedimethanol and 1to 80 mole ethylene glycol; 25 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 75 mole % ethylene glycol; 30 to 99 mole %1,4-cyclohexanedimethanol and 1 to 70 mole % ethylene glycol; 35 to 99mole % 1,4-cyclohexanedimethanol and 1 to 65 mole % ethylene glycol; 40to 99 mole % 1,4-cyclohexanedimethanol and 1 to 60 mole % ethyleneglycol; 45 to 99 mole 1,4-cyclohexanedimethanol and 1 to 55 mole %ethylene glycol; 50 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 50mole % ethylene glycol; 55 to 99 mole % 1,4-cyclohexanedimethanol and 1to 45 mole % ethylene glycol; 60 to 99 mole % 1,4-cyclohexanedimethanoland 1 to 40 mole % ethylene glycol; 65 to 99 mole %1,4-cyclohexanedimethanol and 1 to 35 mole % ethylene glycol; 70 to 99mole % 1,4-cyclohexanedimethanol and 1 to 30 mole ethylene glycol; 75 to99 mole % 1,4-cyclohexanedimethanol and 1 to 25 mole % ethylene glycol;80 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 20 mole % ethyleneglycol; 85 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 15 mole %ethylene glycol; 90 to 99 mole % 1,4-cyclohexanedimethanol and 1 to 10mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 95 mole %1,4-cyclohexanedimethanol and 5 to 99.99 mole % ethylene glycol; 1 to 95mole % 1,4-cyclohexanedimethanol and 5 to 99 mole % ethylene glycol; 5to 95 mole % 1,4-cyclohexanedimethanol and 5 to 95 mole % ethyleneglycol; 10 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 90 mole %ethylene glycol; 15 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 85mole % ethylene glycol; 20 to 95 mole % 1,4-cyclohexanedimethanol and 5to 80 mole % ethylene glycol; 25 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 75 mole % ethylene glycol; 30 to 95 mole %1,4-cyclohexanedimethanol and 5 to 70 mole % ethylene glycol; 35 to 95mole % 1,4-cyclohexanedimethanol and 5 to 65 mole % ethylene glycol; 40to 95 mole % 1,4-cyclohexanedimethanol and 5 to 60 mole % ethyleneglycol; 45 to 95 mole % 1,4-cyclohexanedimethanol and 6 to 55 mole %ethylene glycol; 50 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 50mole % ethylene glycol; 55 to 95 mole % 1,4-cyclohexanedimethanol and 5to 45 mole % ethylene glycol; 60 to 95 mole % 1,4-cyclohexanedimethanoland 5 to 40 mole % ethylene glycol; 65 to 95 mole %1,4-cyclohexanedimethanol and 5 to 35 mole % ethylene glycol; 70 to 95mole % 1,4-cyclohexanedimethanol and 5 to 30 mole % ethylene glycol; 75to 95 mole % 1,4-cyclohexanedimethanol and 5 to 25 mole % ethyleneglycol; 80 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 20 mole %ethylene glycol; 85 to 95 mole % 1,4-cyclohexanedimethanol and 5 to 15mole % ethylene glycol; 90 to 95 mole % 1,4-cyclohexanedimethanol and 5to 10 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 90 mole %1,4-cyclohexanedimethanol and 10 to 99.99 mole % ethylene glycol; 1 to90 mole % 1,4-cyclohexanedimethanol and 10 to 99 mole % ethylene glycol;5 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 95 mole % ethyleneglycol; 10 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 90 mole %ethylene glycol; 15 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 85mole ethylene glycol; 20 to 90 mole % 1,4-cyclohexanedimethanol and 10to 80 mole % ethylene glycol, 25 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 75 mole % ethylene glycol; 30 to 90 mole %1,4-cyclohexanedimethanol and 10 to 70 mole % ethylene glycol; 35 to 90mole % 1,4-cyclohexanedimethanol and 10 to 65 mole % ethylene glycol; 40to 90 mole % 1,4-cyclohexanedimethanol and 10 to 60 mole % ethyleneglycol; 45 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 55 mole %ethylene glycol; 50 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 50mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 90 mole %1,4-cyclohexanedimethanol and 10 to 45 mole % ethylene glycol; 60 to 90mole % 1,4-cyclohexanedimethanol and 10 to 40 mole % ethylene glycol; 65to 90 mole % 1,4-cyclohexanedimethanol and 10 to 35 mole % ethyleneglycol; 70 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 30 mole %ethylene glycol; 75 to 90 mole % 1,4-cyclohexanedimethanol and 10 to 25mole % ethylene glycol; 80 to 90 mole % 1,4-cyclohexanedimethanol and 10to 20 mole % ethylene glycol; 85 to 90 mole % 1,4-cyclohexanedimethanoland 10 to 15 mole ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 85 mole %1,4-cyclohexanedimethanol and 15 to 99.99 mole % ethylene glycol; 1 to85 mole % 1,4-cyclohexanedimethanol and 15 to 99 mole % ethylene glycol;5 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 95 mole % ethyleneglycol; 10 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 90 mole %ethylene glycol; 15 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 85mole % ethylene glycol; 20 to 85 mole % 1,4-cyclohexanedimethanol and 15to 80 mole % ethylene glycol; 25 to 85 mole % 1,4-cyclohexanedimethanoland 15 to 75 mole % ethylene glycol; 30 to 85 mole %1,4-cyclohexanedimethanol and 15 to 70 mole % ethylene glycol; 35 to 85mole % 1,4-cyclohexanedimethanol and 15 to 65 mole % ethylene glycol; 40to 85 mole % 1,4-cyclohexanedimethanol and 15 to 60 mole % ethyleneglycol; 45 to 85 mole % 1,4-cyclohexanedimethanol 15 to 55 mole %ethylene glycol; 50 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 50mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 85 mole %1,4-cyclohexanedimethanol and 15 to 45 mole % ethylene glycol; 60 to 85mole % 1,4-cyclohexanedimethanol and 15 to 40 mole % ethylene glycol; 65to 85 mole % 1,4-cyclohexanedimethanol and 15 to 35 mole % ethyleneglycol; 70 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 30 mole %ethylene glycol; 75 to 85 mole % 1,4-cyclohexanedimethanol and 15 to 25mole % ethylene glycol; 80 to 85 mole % 1,4-cyclohexanedimethanol and 15to 20 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 80 mole %1,4-cyclohexanedimethanol and 20 to 99.99 mole % ethylene glycol; 1 to80 mole % 1,4-cyclohexanedimethanol and 20 to 99 mole % ethylene glycol;5 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 95 mole % ethyleneglycol; 10 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 90 mole %ethylene glycol; 15 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 85mole % ethylene glycol; 20 to 80 mole % 1,4-cyclohexanedimethanol and 20to 80 mole % ethylene glycol; 25 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 75 mole % ethylene glycol; 30 to 80 mole %1,4-cyclohexanedimethanol and 20 to 70 mole % ethylene glycol; 35 to 80mole % 1,4-cyclohexanedimethanol and 20 to 65 mole % ethylene glycol; 40to 80 mole % 1,4-cyclohexanedimethanol and 20 to 60 mole % ethyleneglycol; 45 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 55 mole %ethylene glycol; 50 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 50mole % ethylene glycol; 55 to 80 mole % 1,4-cyclohexanedimethanol and 20to 45 mole % ethylene glycol; 60 to 80 mole % 1,4-cyclohexanedimethanoland 20 to 40 mole % ethylene glycol; 65 to 80 mole %1,4-cyclohexanedimethanol and 20 to 35 mole % ethylene glycol; 70 to 80mole % 1,4-cyclohexanedimethanol and 20 to 30 mole % ethylene glycol;and 75 to 80 mole % 1,4-cyclohexanedimethanol and 20 to 25 mole %ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 75 mole %1,4-cyclohexanedimethanol and 25 to 99.99 mole % ethylene glycol; 1 to75 mole % 1,4-cyclohexanedimethanol and 25 to 99 mole % ethylene glycol;5 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 95 mole % ethyleneglycol; 10 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 90 mole %ethylene glycol; 15 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 85mole % ethylene glycol; 20 to 75 mole % 1,4-cyclohexanedimethanol and 25to 80 mole % ethylene glycol; 25 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 75 mole % ethylene glycol; 30 to 75 mole %1,4-cyclohexanedimethanol and 25 to 70 mole % ethylene glycol; 35 to 75mole % 1,4-cyclohexanedimethanol and 25 to 65 mole % ethylene glycol; 40to 75 mole % 1,4-cyclohexanedimethanol and 25 to 60 mole % ethyleneglycol; 45 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 55 mole %ethylene glycol; 50 to 75 mole % 1,4-cyclohexanedimethanol and 25 to 50mole % ethylene glycol; 55 to 75 mole % 1,4-cyclohexanedimethanol and 25to 45 mole % ethylene glycol; 60 to 75 mole % 1,4-cyclohexanedimethanoland 25 to 40 mole % ethylene glycol; 65 to 75 mole %1,4-cyclohexanedimethanol and 25 to 35 mole % ethylene glycol; and 70 to75 mole % 1,4-cyclohexanedimethanol and 25 to 30 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 70 mole %1,4-cyclohexanedimethanol and 30 to 99.99 mole % ethylene glycol; 1 to70 mole % 1,4-cyclohexanedimethanol and 30 to 99 mole % ethylene glycol;5 to 70 mole % 1,4-cyclohexanedimethanol and 30 to 95 mole % ethyleneglycol; 10 to 70 mole 1,4-cyclohexanedimethanol and 30 to 90 mole %ethylene glycol; 15 to 70 mole % 1,4-cyclohexanedimethanol and 30 to 85mole % ethylene glycol; 20 to 70 mole % 1,4-cyclohexanedimethanol and 30to 80 mole % ethylene glycol; 25 to 70 mole % 1,4-cyclohexanedimethanoland 30 to 75 mole ethylene glycol; 30 to 70 mole %1,4-cyclohexanedimethanol and 30 to 70 mole % ethylene glycol; 35 to 70mole % 1,4-cyclohexanedimethanol and 30 to 65 mole % ethylene glycol; 40to 70 mole % 1,4-cyclohexanedimethanol and 30 to 60 mole % ethyleneglycol; 45 to 70 mole % 1,4-cyclohexanedimethanol and 30 to 55 mole %ethylene glycol; 50 to 70 mole % 1,4-cyclohexanedimethanol and 30 to 50mole % ethylene glycol; 55 to 70 mole % 1,4-cyclohexanedimethanol and 30to 45 mole % ethylene glycol; 60 to 70 mole % 1,4-cyclohexanedimethanoland 30 to 40 mole % ethylene glycol; and 65 to 70 mole %1,4-cyclohexanedimethanol and 30 to 35 mole ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 65 mole %1,4-cyclohexanedimethanol and 35 to 99.99 mole % ethylene glycol; 1 to65 mole % 1,4-cyclohexanedimethanol and 35 to 99 mole % ethylene glycol;5 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 95 mole % ethyleneglycol; 10 to 65 mole 1,4-cyclohexanedimethanol and 35 to 90 mole %ethylene glycol; 15 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 85mole % ethylene glycol; 20 to 65 mole % 1,4-cyclohexanedimethanol and 35to 80 mole % ethylene glycol, 25 to 65 mole % 1,4-cyclohexanedimethanoland 35 to 75 mole ethylene glycol; 30 to 65 mole %1,4-cyclohexanedimethanol and 35 to 70 mole % ethylene glycol; 35 to 65mole % 1,4-cyclohexanedimethanol and 35 to 65 mole % ethylene glycol; 40to 65 mole % 1,4-cyclohexanedimethanol and 35 to 60 mole % ethyleneglycol; 45 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 55 mole %ethylene glycol; 50 to 65 mole % 1,4-cyclohexanedimethanol and 35 to 50mole % ethylene glycol; 55 to 65 mole % 1,4-cyclohexanedimethanol and 35to 45 mole % ethylene glycol; and 60 to 65 mole %1,4-cyclohexanedimethanol and 35 to 40 mole ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 60 mole %1,4-cyclohexanedimethanol and 40 to 99.99 mole % ethylene glycol; 1 to60 mole % 1,4-cyclohexanedimethanol and 40 to 99 mole % ethylene glycol;5 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 95 mole % ethyleneglycol; 10 to 60 mole 1,4-cyclohexanedimethanol and 40 to 90 mole %ethylene glycol; 15 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 85mole % ethylene glycol; 20 to 60 mole % 1,4-cyclohexanedimethanol and 40to 80 mole % ethylene glycol; 25 to 60 mole % 1,4-cyclohexanedimethanoland 40 to 75 mole ethylene glycol; 30 to 60 mole %1,4-cyclohexanedimethanol and 40 to 70 mole % ethylene glycol; 35 to 60mole % 1,4-cyclohexanedimethanol and 40 to 65 mole % ethylene glycol; 40to 60 mole % 1,4-cyclohexanedimethanol and 40 to 60 mole % ethyleneglycol; 45 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 55 mole %ethylene glycol; 50 to 60 mole % 1,4-cyclohexanedimethanol and 40 to 50mole % ethylene glycol; 55 to 60 mole % 1,4-cyclohexanedimethanol and 40to 45 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 55 mole %1,4-cyclohexanedimethanol and 45 to 99.99 mole % ethylene glycol; 1 to55 mole % 1,4-cyclohexanedimethanol and 45 to 99 mole % ethylene glycol;5 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 95 mole % ethyleneglycol; 10 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 90 mole %ethylene glycol; 15 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 85mole % ethylene glycol; 20 to 55 mole % 1,4-cyclohexanedimethanol and 45to 80 mole % ethylene glycol; 25 to 55 mole % 1,4-cyclohexanedimethanoland 45 to 75 mole % ethylene glycol; 30 to 55 mole %1,4-cyclohexanedimethanol and 45 to 70 mole % ethylene glycol; 35 to 55mole % 1,4-cyclohexanedimethanol and 45 to 65 mole % ethylene glycol; 40to 55 mole % 1,4-cyclohexanedimethanol and 45 to 60 mole % ethyleneglycol; 45 to 55 mole % 1,4-cyclohexanedimethanol and 45 to 55 mole %ethylene glycol; and 50 to 55 mole % 1,4-cyclohexanedimethanol and 45 to50 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 50 mole %1,4-cyclohexanedimethanol and 50 to 99.99 mole % ethylene glycol; 1 to50 mole % 1,4-cyclohexanedimethanol and 50 to 99 mole % ethylene glycol;5 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 95 mole % ethyleneglycol; 10 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 90 mole %ethylene glycol; 15 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 85mole % ethylene glycol; 20 to 50 mole % 1,4-cyclohexanedimethanol and 50to 80 mole % ethylene glycol 25 to 50 mole % 1,4-cyclohexanedimethanoland 50 to 75 mole % ethylene glycol; 30 to 50 mole %1,4-cyclohexanedimethanol and 50 to 70 mole % ethylene glycol; 35 to 50mole % 1,4-cyclohexanedimethanol and 50 to 65 mole % ethylene glycol; 40to 50 mole % 1,4-cyclohexanedimethanol and 50 to 60 mole % ethyleneglycol; and 45 to 50 mole % 1,4-cyclohexanedimethanol and 50 to 55 mole% ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 45 mole %1,4-cyclohexanedimethanol and 55 to 99.99 mole % ethylene glycol; 1 to45 mole % 1,4-cyclohexanedimethanol and 55 to 99 mole % ethylene glycol;5 to 45 mole % 1,4-cyclohexanedimethanol and 50 to 95 mole % ethyleneglycol; 10 to 45 and 55 to 95 mole % ethylene glycol mole %1,4-cyclohexanedimethanol; 15 to 45 mole % 1,4-cyclohexanedimethanol and55 to 85 mole % ethylene glycol; 20 to 45 mole %1,4-cyclohexanedimethanol and 55 to 80 mole % ethylene glycol; 25 to 45mole % 1,4-cyclohexanedimethanol and 55 to 75 mole % ethylene glycol; 30to 45 mole % 1,4-cyclohexanedimethanol and 55 to 65 mole % ethyleneglycol; 35 to 45 mole % 1,4-cyclohexanedimethanol and 55 to 65 mole %ethylene glycol; 40 to 45 mole % 1,4-cyclohexanedimethanol and 55 to 60mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 40 mole %1,4-cyclohexanedimethanol and 60 to 99.99 mole % ethylene glycol; 1 to40 mole % 1,4-cyclohexanedimethanol and 60 to 99 mole % ethylene glycol;5 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 95 mole % ethyleneglycol; 10 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 90 mole %ethylene glycol; 15 to 40 mole % 1,4-cyclohexanedimethanol and 60 to 85mole % ethylene glycol; 20 to 40 mole % 1,4-cyclohexanedimethanol and 60to 80 mole % ethylene glycol; 25 to 40 mole % 1,4-cyclohexanedimethanoland 60 to 75 mole % ethylene glycol; 30 to 40 mole %1,4-cyclohexanedimethanol and 60 to 70 mole % ethylene glycol; 35 to 40mole % 1,4-cyclohexanedimethanol and 60 to 65 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 35 mole %1,4-cyclohexanedimethanol and 65 to 99.99 mole % ethylene glycol; 1 to35 mole % 1,4-cyclohexanedimethanol and 65 to 99 mole % ethylene glycol;5 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 95 mole % ethyleneglycol; 10 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 90 mole %ethylene glycol; 15 to 35 mole % 1,4-cyclohexanedimethanol and 65 to 85mole % ethylene glycol; 20 to 35 mole % 1,4-cyclohexanedimethanol and 65to 80 mole % ethylene gycol; 25 to 35 mole % 1,4-cyclohexanedimethanoland 65 to 75 mole % ethylene glycol; 30 to 35 mole %1,4-cyclohexanedimethanol and 65 to 70 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 30 mole %1,4-cyclohexanedimethanol and 70 to 99.99 mole % mole % ethylene glycol;1 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 99 mole % ethyleneglycol; 5 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 95 mole %ethylene glycol; 10 to 30 mole % 1,4-cyclohexanedimethanol and 70 to 90mole % ethylene glycol; 15 to 30 mole % 1,4-cyclohexanedimethanol and 70to 85 mole % ethylene glycol; 20 to 30 mole % 1,4-cyclohexanedimethanoland 70 to 80 mole % ethylene glycol; 25 to 30 mole %1,4-cyclohexanedimethanol and 70 to 75 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 25 mole %1,4-cyclohexanedimethanol and 75 to 99.99 mole % ethylene glycol; 1 to25 mole % 1,4-cyclohexanedimethanol and 75 to 99 mole % ethylene glycol;5 to 25 mole % 1,4-cyclohexanedimethanol and 75 to 95 mole % ethyleneglycol; 10 to 25 mole % 1,4-cyclohexanedimethanol and 75 to 90 mole %ethylene glycol; 15 to 25 mole % 1,4-cyclohexanedimethanol and 75 to 85mole % ethylene glycol; 20 to 25 mole % 1,4-cyclohexanedimethanol and 75to 80 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 20 mole %1,4-cyclohexanedimethanol and 80 to 99.99 mole % ethylene glycol; 1 to20 mole % 1,4-cyclohexanedimethanol and 80 to 99 mole % ethylene glycol;5 to 20 mole % 1,4-cyclohexanedimethanol and 80 to 95 mole % ethyleneglycol; 10 to 20 mole % 1,4-cyclohexanedimethanol and 80 to 90 mole %ethylene glycol; and 15 to 20 mole % 1,4-cyclohexanedimethanol and 80 to85 mole % ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 15 mole %1,4-cyclohexanedimethanol and 85 to 99.99 mole % ethylene glycol; 1 to15 mole % 1,4-cyclohexanedimethanol and 85 to 99 mole % ethylene glycol;5 to 15 mole % 1,4-cyclohexanedimethanol and 85 to 95 mole % ethyleneglycol; and 10 to 15 mole % 1,4-cyclohexanedimethanol and 85 to 90 mole% ethylene glycol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 10 mole %1,4-cyclohexanedimethanol and 90 to 99.99 mole % ethylene glycol; 1 to10 mole % 1,4-cyclohexanedimethanol and 90 to 99 mole % ethylene glycol;5 to 10 mole % 1,4-cyclohexanedimethanol and 90 to 95 mole % ethyleneglycol; 0.01 to 5 mole % 1,4-cyclohexanedimethanol and 95 to 99.99 mole% ethylene glycol and 1 to 5 mole % 1,4-cyclohexanedimethanol and 95 to99 mole % ethylene glycol.

The polyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 99 mole %1,4-cyclohexanedimethanol and 1 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 99 mole %1,4-cyclohexanedimethanol and 1 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 99 mole %1,4-cyclohexanedimethanol and 1 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 99 mole %1,4-cyclohexanedimethanol and 1 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 99 mole %1,4-cyclohexanedimethanol and 1 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 99 mole %1,4-cyclohexanedimethanol and 1 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 99 mole %1,4-cyclohexanedimethanol and 1 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 99 mole %1,4-cyclohexanedimethanol and 1 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 99 mole %1,4-cyclohexanedimethanol and 1 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 99 mole %1,4-cyclohexanedimethanol and 1 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 99 mole %1,4-cyclohexanedimethanol and 1 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 99 mole %1,4-cyclohexanedimethanol and 1 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 99 mole %1,4-cyclohexanedimethanol and 1 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 99 mole %1,4-cyclohexanedimethanol and 1 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 99 mole %1,4-cyclohexanedimethanol and 1 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 70 to 99 mole %1,4-cyclohexanedimethanol and 1 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 75 to 99 mole %1,4-cyclohexanedimethanol and 1 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 80 to 99 mole %1,4-cyclohexanedimethanol and 1 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 85 to 99 mole %1,4-cyclohexanedimethanol and 1 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 90 to 99 mole %1,4-cyclohexanedimethanol and 1 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 95 to 99 mole %1,4-cyclohexanedimethanol and 1 to 5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 90 to less than 99.99 mole %1,4-cyclohexanedimethanol and 0.01 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 95 to less than 99.99 mole %1,4-cyclohexanedimethanol and 0.01 to 5 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 95 mole %1,4-cyclohexanedimethanol and 5 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 95 mole %1,4-cyclohexanedimethanol and 5 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 95 mole %1,4-cyclohexanedimethanol and 5 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 95 mole %1,4-cyclohexanedimethanol and 5 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 95 mole %1,4-cyclohexanedimethanol and 5 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 95 mole %1,4-cyclohexanedimethanol and 5 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 95 mole %1,4-cyclohexanedimethanol and 5 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 95 mole %1,4-cyclohexanedimethanol and 5 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 95 mole %1,4-cyclohexanedimethanol and 5 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 95 mole %1,4-cyclohexanedimethanol and 5 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 95 mole %1,4-cyclohexanedimethanol and 5 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 95 mole %1,4-cyclohexanedimethanol and 5 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 95 mole %1,4-cyclohexanedimethanol and 5 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 95 mole %1,4-cyclohexanedimethanol and 5 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 95 mole %1,4-cyclohexanedimethanol and 5 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 70 to 95 mole %1,4-cyclohexanedimethanol and 5 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 75 to 95 mole %1,4-cyclohexanedimethanol and 5 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 80 to 95 mole %1,4-cyclohexanedimethanol and 5 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 85 to 95 mole %1,4-cyclohexanedimethanol and 5 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 90 to 95 mole %1,4-cyclohexanedimethanol and 5 to 10 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the film or sheet of the invention include but arenot limited to at least one of the following ranges: 0.01 to 90 mole %1,4-cyclohexanedimethanol and 10 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 90 mole %1,4-cyclohexanedimethanol and 10 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 90 mole %1,4-cyclohexanedimethanol and 10 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 90 mole %1,4-cyclohexanedimethanol and 10 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 90 mole %1,4-cyclohexanedimethanol and 10 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 90 mole %1,4-cyclohexanedimethanol and 10 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol, 25 to 90 mole %1,4-cyclohexanedimethanol and 10 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 90 mole %1,4-cyclohexanedimethanol and 10 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 90 mole %1,4-cyclohexanedimethanol and 10 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 90 mole %1,4-cyclohexanedimethanol and 10 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 90 mole %1,4-cyclohexanedimethanol and 10 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 90 mole %1,4-cyclohexanedimethanol and 10 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 90 mole %1,4-cyclohexanedimethanol and 10 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 90 mole %1,4-cyclohexanedimethanol and 10 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 90 mole %1,4-cyclohexanedimethanol and 10 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 70 to 90 mole %1,4-cyclohexanedimethanol and 10 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 75 to 90 mole %1,4-cyclohexanedimethanol and 10 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 80 to 90 mole %1,4-cyclohexanedimethanol and 10 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 85 to 90 mole %1,4-cyclohexanedimethanol and 10 to 15 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 85 mole %1,4-cyclohexanedimethanol and 15 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 85 mole %1,4-cyclohexanedimethanol and 15 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 85 mole %1,4-cyclohexanedimethanol and 15 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 85 mole %1,4-cyclohexanedimethanol and 15 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 85 mole %1,4-cyclohexanedimethanol and 15 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 85 mole %1,4-cyclohexanedimethanol and 15 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 85 mole %1,4-cyclohexanedimethanol and 15 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 85 mole %1,4-cyclohexanedimethanol and 15 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 85 mole %1,4-cyclohexanedimethanol and 15 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 85 mole %1,4-cyclohexanedimethanol and 15 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 85 mole %1,4-cyclohexanedimethanol 15 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 85 mole %1,4-cyclohexanedimethanol and 15 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 55 to 85 mole %1,4-cyclohexanedimethanol and 15 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 85 mole %1,4-cyclohexanedimethanol and 15 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 85 mole %1,4-cyclohexanedimethanol and 15 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 70 to 85 mole %1,4-cyclohexanedimethanol and 15 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 75 to 85 mole %1,4-cyclohexanedimethanol and 15 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 80 to 85 mole %1,4-cyclohexanedimethanol and 15 to 20 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 80 mole %1,4-cyclohexanedimethanol and 20 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 80 mole %1,4-cyclohexanedimethanol and 20 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 80 mole %1,4-cyclohexanedimethanol and 20 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 80 mole %1,4-cyclohexanedimethanol and 20 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 80 mole %1,4-cyclohexanedimethanol and 20 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 80 mole %1,4-cyclohexanedimethanol and 20 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 80 mole %1,4-cyclohexanedimethanol and 20 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 80 mole %1,4-cyclohexanedimethanol and 20 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 80 mole %1,4-cyclohexanedimethanol and 20 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 80 mole %1,4-cyclohexanedimethanol and 20 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 80 mole %1,4-cyclohexanedimethanol and 20 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 80 mole %1,4-cyclohexanedimethanol and 20 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 80 mole %1,4-cyclohexanedimethanol and 20 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 80 mole %1,4-cyclohexanedimethanol and 20 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 80 mole %1,4-cyclohexanedimethanol and 20 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 70 to 80 mole %1,4-cyclohexanedimethanol and 20 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 75 to 80 mole %1,4-cyclohexanedimethanol and 20 to 25 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 75 mole %1,4-cyclohexanedimethanol and 25 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 75 mole %1,4-cyclohexanedimethanol and 25 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 75 mole %1,4-cyclohexanedimethanol and 25 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 75 mole %1,4-cyclohexanedimethanol and 25 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 75 mole %1,4-cyclohexanedimethanol and 25 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 75 mole %1,4-cyclohexanedimethanol and 25 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 75 mole %1,4-cyclohexanedimethanol and 25 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 75 mole %1,4-cyclohexanedimethanol and 25 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 75 mole %1,4-cyclohexanedimethanol and 25 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 75 mole %1,4-cyclohexanedimethanol and 25 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 75 mole %1,4-cyclohexanedimethanol and 25 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 75 mole %1,4-cyclohexanedimethanol and 25 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 75 mole %1,4-cyclohexanedimethanol and 25 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 60 to 75 mole %1,4-cyclohexanedimethanol and 25 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 65 to 75 mole %1,4-cyclohexanedimethanol and 25 to 35 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 70 to 75 mole %1,4-cyclohexanedimethanol and 25 to 30 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 65 mole %1,4-cyclohexanedimethanol and 35 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 65 mole %1,4-cyclohexanedimethanol and 35 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 65 mole %1,4-cyclohexanedimethanol and 35 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 65 mole %1,4-cyclohexanedimethanol and 35 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 65 mole %1,4-cyclohexanedimethanol and 35 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 65 mole %1,4-cyclohexanedimethanol and 35 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol, 25 to 65 mole %1,4-cyclohexanedimethanol and 35 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 65 mole %1,4-cyclohexanedimethanol and 35 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 65 mole %1,4-cyclohexanedimethanol and 35 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 65 mole %1,4-cyclohexanedimethanol and 35 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 65 mole %1,4-cyclohexanedimethanol and 35 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 65 mole %1,4-cyclohexanedimethanol and 35 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 65 mole %1,4-cyclohexanedimethanol and 35 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 60 to 65 mole %1,4-cyclohexanedimethanol and 35 to 40 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 60 mole %1,4-cyclohexanedimethanol and 40 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 60 mole %1,4-cyclohexanedimethanol and 40 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 60 mole %1,4-cyclohexanedimethanol and 40 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 60 mole %1,4-cyclohexanedimethanol and 40 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 60 mole %1,4-cyclohexanedimethanol and 40 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 60 mole %1,4-cyclohexanedimethanol and 40 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 60 mole %1,4-cyclohexanedimethanol and 40 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 60 mole %1,4-cyclohexanedimethanol and 40 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 60 mole %1,4-cyclohexanedimethanol and 40 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 60 mole %1,4-cyclohexanedimethanol and 40 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 60 mole %1,4-cyclohexanedimethanol and 40 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 50 to 60 mole %1,4-cyclohexanedimethanol and 40 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 55 to 60 mole %1,4-cyclohexanedimethanol and 40 to 45 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 55 mole %1,4-cyclohexanedimethanol and 45 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 55 mole %1,4-cyclohexanedimethanol and 45 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 55 mole %1,4-cyclohexanedimethanol and 45 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 55 mole %1,4-cyclohexanedimethanol and 45 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 55 mole %1,4-cyclohexanedimethanol and 45 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 55 mole %1,4-cyclohexanedimethanol and 45 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 55 mole %1,4-cyclohexanedimethanol and 45 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 55 mole %1,4-cyclohexanedimethanol and 45 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 55 mole %1,4-cyclohexanedimethanol and 45 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 55 mole %1,4-cyclohexanedimethanol and 45 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 45 to 55 mole %1,4-cyclohexanedimethanol and 45 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 50 to 55 mole %1,4-cyclohexanedimethanol and 45 to 50 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 50 mole %1,4-cyclohexanedimethanol and 50 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 50 mole %1,4-cyclohexanedimethanol and 50 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 50 mole %1,4-cyclohexanedimethanol and 50 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 50 mole %1,4-cyclohexanedimethanol and 50 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 50 mole %1,4-cyclohexanedimethanol and 50 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 50 mole %1,4-cyclohexanedimethanol and 50 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol 25 to 50 mole %1,4-cyclohexanedimethanol and 50 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 50 mole %1,4-cyclohexanedimethanol and 50 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 50 mole %1,4-cyclohexanedimethanol and 50 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 50 mole %1,4-cyclohexanedimethanol and 50 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 45 to 50 mole %1,4-cyclohexanedimethanol and 50 to 55 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 45 mole %1,4-cyclohexanedimethanol and 55 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 45 mole %1,4-cyclohexanedimethanol and 55 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 45 mole %1,4-cyclohexanedimethanol and 50 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 45 and 55 to 95 mole2,2,4,4-tetramethyl-1,3-cyclobutanediol mole %1,4-cyclohexanedimethanol; 15 to 45 mole % 1,4-cyclohexanedimethanol and55 to 85 mole % 2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 45 mole %1,4-cyclohexanedimethanol and 55 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 45 mole %1,4-cyclohexanedimethanol and 55 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 45 mole %1,4-cyclohexanedimethanol and 55 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 45 mole %1,4-cyclohexanedimethanol and 55 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 40 to 45 mole %1,4-cyclohexanedimethanol and 55 to 60 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 40 mole %1,4-cyclohexanedimethanol and 60 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 40 mole %1,4-cyclohexanedimethanol and 60 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 40 mole %1,4-cyclohexanedimethanol and 60 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 40 mole %1,4-cyclohexanedimethanol and 60 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 40 mole %1,4-cyclohexanedimethanol and 60 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 40 mole %1,4-cyclohexanedimethanol and 60 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 40 mole %1,4-cyclohexanedimethanol and 60 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 40 mole %1,4-cyclohexanedimethanol and 60 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 35 to 40 mole %1,4-cyclohexanedimethanol and 60 to 65 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 35 mole %1,4-cyclohexanedimethanol and 65 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 35 mole %1,4-cyclohexanedimethanol and 65 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 35 mole %1,4-cyclohexanedimethanol and 65 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 35 mole %1,4-cyclohexanedimethanol and 65 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 35 mole %1,4-cyclohexanedimethanol and 65 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 35 mole %1,4-cyclohexanedimethanol and 65 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 35 mole %1,4-cyclohexanedimethanol and 65 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 30 to 35 mole %1,4-cyclohexanedimethanol and 65 to 70 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 30 mole %1,4-cyclohexanedimethanol and 70 to 99.99 mole % mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 30 mole %1,4-cyclohexanedimethanol and 70 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 30 mole %1,4-cyclohexanedimethanol and 70 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 30 mole %1,4-cyclohexanedimethanol and 70 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 30 mole %1,4-cyclohexanedimethanol and 70 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 30 mole %1,4-cyclohexanedimethanol and 70 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 25 to 30 mole %1,4-cyclohexanedimethanol and 70 to 75 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 25 mole %1,4-cyclohexanedimethanol and 75 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 25 mole %1,4-cyclohexanedimethanol and 75 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 25 mole %1,4-cyclohexanedimethanol and 75 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 25 mole %1,4-cyclohexanedimethanol and 75 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 15 to 25 mole %1,4-cyclohexanedimethanol and 75 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 20 to 25 mole %1,4-cyclohexanedimethanol and 75 to 80 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 20 mole %1,4-cyclohexanedimethanol and 80 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 20 mole %1,4-cyclohexanedimethanol and 80 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 20 mole %1,4-cyclohexanedimethanol and 80 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 10 to 20 mole %1,4-cyclohexanedimethanol and 80 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 15 to 20 mole %1,4-cyclohexanedimethanol and 80 to 85 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 15 mole %1,4-cyclohexanedimethanol and 85 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 15 mole %1,4-cyclohexanedimethanol and 85 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 15 mole %1,4-cyclohexanedimethanol and 85 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; and 10 to 15 mole %1,4-cyclohexanedimethanol and 85 to 90 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

In other aspects of the invention, the glycol component for thepolyesters useful in the invention include but are not limited to atleast one of the following ranges: 0.01 to 10 mole %1,4-cyclohexanedimethanol and 90 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 1 to 10 mole %1,4-cyclohexanedimethanol and 90 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 5 to 10 mole %1,4-cyclohexanedimethanol and 90 to 95 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol; 0.01 to 5 mole %1,4-cyclohexanedimethanol and 95 to 99.99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1 to 5 mole %1,4-cyclohexanedimethanol and 95 to 99 mole %2,2,4,4-tetramethyl-1,3-cyclobutanediol.

For certain embodiments of the invention, the polyesters useful in theinvention may exhibit at least one of the following inherent viscositiesas determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.: 0.10 to 1.2 dL/g; 0.10 to 1.1dL/g; 0.10 to 1 dL/g; 0.10 to less than 1 dL/g; 0.10 to 0.98 dL/g; 0.10to 0.95 dL/g; 0.10 to 0.90 dL/g; 0.10 to 0.85 dL/g; 0.10 to 0.80 dL/g;0.10 to 0.75 dL/g; 0.10 to less than 0.75 dL/g; 0.10 to 0.72 dL/g; 0.10to 0.70 dL/g; 0.10 to less than 0.70 dL/g; 0.10 to 0.68 dL/g; 0.10 toless than 0.68 dL/g; 0.10 to 0.65 dL/g; 0.20 to 1.2 dL/g; 0.20 to 1.1dL/g; 0.20 to 1 dL/g; 0.20 to less than 1 dL/g; 0.20 to 0.98 dL/g; 0.20to 0.95 dL/g; 0.20 to 0.90 dL/g; 0.20 to 0.85 dL/g; 0.20 to 0.80 dL/g;0.20 to 0.75 dL/g; 0.20 to less than 0.75 dL/g; 0.20 to 0.72 dL/g; 0.20to 0.70 dL/g; 0.20 to less than 0.70 dL/g; 0.20 to 0.68 dL/g; 0.20 toless than 0.68 dL/g; 0.20 to 0.65 dL/g; 0.35 to 1.2 dL/g; 0.35 to 1.1dL/g; 0.35 to 1 dL/g; 0.35 to less than 1 dL/g; 0.35 to 0.98 dL/g; 0.35to 0.95 dL/g; 0.35 to 0.90 dL/g; 0.35 to 0.85 dL/g; 0.35 to 0.80 dL/g;0.35 to 0.75 dL/g; 0.35 to less than 0.75 dL/g; 0.35 to 0.72 dL/g; 0.35to 0.70 dL/g; 0.35 to less than 0.70 dL/g; 0.35 to 0.68 dL/g; 0.35 toless than 0.68 dL/g; 0.35 to 0.65 dL/g; 0.40 to 1.2 dL/g; 0.40 to 1.1dL/g; 0.40 to 1 dL/g; 0.40 to less than 1 dL/g; 0.40 to 0.98 dL/g; 0.40to 0.95 dL/g; 0.40 to 0.90 dL/g; 0.40 to 0.85 dL/g; 0.40 to 0.80 dL/g;0.40 to 0.75 dL/g; 0.40 to less than 0.75 dL/g; 0.40 to 0.72 dL/g; 0.40to 0.70 dL/g; 0.40 to less than 0.70 dL/g; 0.40 to 0.68 dL/g; 0.40 toless than 0.68 dL/g; 0.40 to 0.65 dL/g; greater than 0.42 to 1.2 dL/g;greater than 0.42 to 1.1 dL/g; greater than 0.42 to 1 dL/g; greater than0.42 to less than 1 dL/g; greater than 0.42 to 0.98 dL/g; greater than0.42 to 0.95 dL/g; greater than 0.42 to 0.90 dL/g; greater than 0.42 to0.85 dL/g; greater than 0.42 to 0.80 dL/g; greater than 0.42 to 0.75dL/g; greater than 0.42 to less than 0.75 dL/g; greater than 0.42 to0.72 dL/g; greater than 0.42 to less than 0.70 dL/g; greater than 0.42to 0.68 dL/g; greater than 0.42 to less than 0.68 dL/g; and greater than0.42 to 0.65 dL/g.

For certain embodiments of the invention, the polyesters useful in theinvention may exhibit at least one of the following inherent viscositiesas determined in 60/40 (wt/wt) phenol/tetrachloroethane at aconcentration of 0.5 g/100 ml at 25° C.: 0.45 to 1.2 dL/g; 0.45 to 1.1dL/g; 0.45 to 1 dL/g; 0.45 to 0.98 dL/g; 0.45 to 0.95 dL/g; 0.45 to 0.90dL/g; 0.45 to 0.85 dL/g; 0.45 to 0.80 dL/g; 0.45 to 0.75 dL/g; 0.45 toless than 0.75 dL/g; 0.45 to 0.72 dL/g; 0.45 to 0.70 dL/g; 0.45 to lessthan 0.70 dL/g; 0.45 to 0.68 dL/g; 0.45 to less than 0.68 dL/g; 0.45 to0.65 dL/g; 0.50 to 1.2 dL/g; 0.50 to 1.1 dL/g; 0.50 to 1 dL/g; 0.50 toless than 1 dL/g; 0.50 to 0.98 dL/g; 0.50 to 0.95 dL/g; 0.50 to 0.90dL/g; 0.50 to 0.85 dL/g; 0.50 to 0.80 dL/g; 0.50 to 0.75 dL/g; 0.50 toless than 0.75 dL/g; 0.50 to 0.72 dL/g; 0.50 to 0.70 dL/g; 0.50 to lessthan 0.70 dL/g; 0.50 to 0.68 dL/g; 0.50 to less than 0.68 dL/g; 0.50 to0.65 dL/g; 0.55 to 1.2 dL/g; 0.55 to 1.1 dL/g; 0.55 to 1 dL/g; 0.55 toless than 1 dL/g; 0.55 to 0.98 dL/g; 0.55 to 0.95 dL/g; 0.55 to 0.90dL/g; 0.55 to 0.85 dL/g; 0.55 to 0.80 dL/g; 0.55 to 0.75 dL/g; 0.55 toless than 0.75 dL/g; 0.55 to 0.72 dL/g; 0.55 to 0.70 dL/g; 0.55 to lessthan 0.70 dL/g; 0.55 to 0.68 dL/g; 0.55 to less than 0.68 dL/g; 0.55 to0.65 dL/g; 0.58 to 1.2 dL/g; 0.58 to 1.1 dL/g; 0.58 to 1 dL/g; 0.58 toless than 1 dL/g; 0.58 to 0.98 dL/g; 0.58 to 0.95 dL/g; 0.58 to 0.90dL/g; 0.58 to 0.85 dL/g; 0.58 to 0.80 dL/g; 0.58 to 0.75 dL/g; 0.58 toless than 0.75 dL/g; 0.58 to 0.72 dL/g; 0.58 to 0.70 dL/g; 0.58 to lessthan 0.70 dL/g; 0.58 to 0.68 dL/g; 0.58 to less than 0.68 dL/g; 0.58 to0.65 dL/g; 0.60 to 1.2 dL/g; 0.60 to 1.1 dL/g; 0.60 to 1 dL/g; 0.60 toless than 1 dL/g; 0.60 to 0.98 dL/g; 0.60 to 0.95 dL/g; 0.60 to 0.90dL/g; 0.60 to 0.85 dL/g; 0.60 to 0.80 dL/g; 0.60 to 0.75 dL/g; 0.60 toless than 0.75 dL/g; 0.60 to 0.72 dL/g; 0.60 to 0.70 dL/g; 0.60 to lessthan 0.70 dL/g; 0.60 to 0.68 dL/g; 0.60 to less than 0.68 dL/g; 0.60 to0.65 dL/g; 0.65 to 1.2 dL/g; 0.65 to 1.1 dL/g; 0.65 to 1 dL/g; 0.65 toless than 1 dL/g; 0.65 to 0.98 dL/g; 0.65 to 0.95 dL/g; 0.65 to 0.90dL/g; 0.65 to 0.85 dL/g; 0.65 to 0.80 dL/g; 0.65 to 0.75 dL/g; 0.65 toless than 0.75 dL/g; 0.65 to 0.72 dL/g; 0.65 to 0.70 dL/g; 0.65 to lessthan 0.70 dL/g; 0.68 to 1.2 dL/g; 0.68 to 1.1 dL/g; 0.68 to 1 dL/g; 0.68to less than 1 dL/g; 0.68 to 0.98 dL/g; 0.68 to 0.95 dL/g; 0.68 to 0.90dL/g; 0.68 to 0.85 dL/g; 0.68 to 0.80 dL/g; 0.68 to 0.75 dL/g; 0.68 toless than 0.75 dL/g; 0.68 to 0.72 dL/g; greater than 0.76 dL/g to 1.2dL/g; greater than 0.76 dL/g to 1.1 dL/g; greater than 0.76 dL/g to 1dL/g; greater than 0.76 dL/g to less than 1 dL/g; greater than 0.76 dL/gto 0.98 dL/g; greater than 0.76 dL/g to 0.95 dL/g; greater than 0.76dL/g to 0.90 dL/g; greater than 0.80 dL/g to 1.2 dL/g; greater than 0.80dL/g to 1.1 dL/g; greater than 0.80 dL/g to 1 dL/g; greater than 0.80dL/g to less than 1 dL/g; greater than 0.80 dL/g to 1.2 dL/g; greaterthan 0.80 dL/g to 0.98 dL/g; greater than 0.80 dL/g to 0.95 dL/g;greater than 0.80 dL/g to 0.90 dL/g.

It is contemplated that the polyester compositions of the invention canpossess at least one of the inherent viscosity ranges described hereinand at least one of the monomer ranges for the compositions describedherein unless otherwise stated. It is also contemplated that thepolyester compositions of the invention can posses at least one of theTg ranges described herein and at least one of the monomer ranges forthe compositions described herein unless otherwise stated. It is alsocontemplated that the polyester compositions of the invention can possesat least one of the Tg ranges described herein, at least one of theinherent viscosity ranges described herein, and at least one of themonomer ranges for the compositions described herein unless otherwisestated.

In certain embodiments, furandicarboxylic acid, or an ester thereof or amixture of furandicarboxylic acid and an ester thereof, makes up most orall of the dicarboxylic acid component used to form the polyestersuseful in the invention. In certain embodiments, 2,5-furandicarboxylicacid residues and/or its ester can be present at a concentration of atleast 70 mole %, such as at least 80 mole %, at least 90 mole %, atleast 95 mole %, at least 99 mole %, or 100 mole %. For purposes of thisdisclosure, the terms “2,5-furandicarboxylic acid” and its esters areused interchangeably herein. In certain embodiments, ranges of from 70to 100 mole %; or 80 to 100 mole %; or 90 to 100 mole %; or 99 to 100mole %; or 100 mole % 2,5-furandicarboxylic acid and/or its esters maybe used. In certain embodiments, ranges of from 70 to 100 mole %; or 80to 100 mole %; or 90 to 100 mole %; or 99 to 100 mole %; or 100 mole %2,5-furandicarboxylic acid and/or its esters may be used.

In addition to 2,5-furandicarboxylic acid residues, the dicarboxylicacid component of the polyesters useful in the invention can comprise upto 30 mole %, up to 20 mole %, up to 10 mole %, up to 5 mole %, or up to1 mole % of one or more modifying aromatic dicarboxylic acids. Yetanother embodiment contains 0 mole % modifying aromatic dicarboxylicacids. Thus, if present, it is contemplated that the amount of one ormore modifying aromatic dicarboxylic acids can range from any of thesepreceding endpoint values including, for example, from 0.01 to 30 mole%, from 0.01 to 20 mole %, from 0.01 to 10 mole %, from 0.01 to 5 mole%, or from 0.01 to 1 mole % of one or more modifying aromaticdicarboxylic acids. In one embodiment, modifying aromatic dicarboxylicacids that may be used in the present invention include but are notlimited to those having up to 20 carbon atoms, and that can be linear,para-oriented, or symmetrical. Examples of modifying aromaticdicarboxylic acids which may be used in this invention include, but arenot limited to, terephthalic acid, isophthalic acid,4,4′-biphenyldicarboxylic acid, 1,4-, 1,5-, 2,6-,2,7-naphthalenedicarboxylic acid, and trans-4,4′-stilbenedicarboxylicacid, and esters thereof. In one embodiment, isophthalic acid is themodifying aromatic dicarboxylic acid. In one embodiment, terephthalicacid is the modifying aromatic dicarboxylic acid.

The carboxylic acid component of the polyesters useful in the inventioncan be further modified with up to 30 mole %, such as up to 25 mole % orsuch as up to such as up to 20 mole % or such as up to 15 mole % or suchas up to 10 mole % or such as up to 5 mole % or up to 1 mole % of one ormore aliphatic dicarboxylic acids containing 2-16 carbon atoms, such as,for example, malonic, succinic, glutaric, adipic, pimelic, suberic,azelaic and dodecanedioic dicarboxylic acids. Certain embodiments canalso comprise 0.01 or more mole %, such as 0.1 or more mole %, 1 or moremole %, 5 or more mole %, or 10 or more mole % of one or more modifyingaliphatic dicarboxylic acids. Yet another embodiment contains 0 mole %modifying aliphatic dicarboxylic acids. Thus, if present, it iscontemplated that the amount of one or more modifying aliphaticdicarboxylic acids can range from any of these preceding endpoint valuesincluding, for example, from 0.01 to 10 mole % and from 0.1 to 10 mole%. The total mole % of the dicarboxylic acid component is 100 mole %.

Esters of terephthalic acid and the other modifying dicarboxylic acidsor their corresponding esters and/or salts may be used instead of thedicarboxylic acids. Suitable examples of dicarboxylic acid estersinclude, but are not limited to, the dimethyl, diethyl, dipropyl,diisopropyl, dibutyl, and diphenyl esters. In one embodiment, the estersare chosen from at least one of the following: methyl, ethyl, propyl,isopropyl, and phenyl esters.

The 1,4-cyclohexanedimethanol may be cis, trans, or a mixture thereof,for example, a cis/trans ratio of 60:40 to 40:60. In another embodiment,the trans-1,4-cyclohexanedimethanol can be present in the amount of 60to 80 mole %. For the desired polyester, the molar ratio of cis/trans2,2,4,4-tetramethyl-1,3-cyclobutanediol can vary within the range of50/50 to 100/0, for example, between 40/60 to 60/40. In certainembodiments, the amount of cis-2,2,4,4-tetramethyl-1,3-cyclobutanediolis greater than 50 mole %, or greater than 55 mole % or greater than 60mole or greater than 65 mole % or greater than 70 mole % or greater than75 mole %.

The glycol component of the polyester portion of the polyestercompositions useful in the invention contain no more than 98 mole % ofmodifying glycols (glycols other than CHDM). In one embodiment, thepolyesters useful in the invention can contain less than 30 mole % ofone or more modifying glycols. In one embodiment, the polyesters usefulin the invention can contain less than 25 mole % of one or moremodifying glycols. In one embodiment, the polyesters useful in theinvention can contain less than 20 mole % of one or more modifyingglycols. In one embodiment, the polyesters useful in the invention cancontain less than 15 mole % of one or more modifying glycols. In anotherembodiment, the polyesters useful in the invention can contain 10 mole %or less of one or more modifying glycols. In another embodiment, thepolyesters useful in the invention can contain 5 mole % or less of oneor more modifying glycols. In another embodiment, the polyesters usefulin the invention can contain 3 mole % or less of one or more modifyingglycols. In another embodiment, the polyesters useful in the inventionmay contain 0 mole % modifying glycols. Certain embodiments can alsocontain 0.01 or more mole %, such as 0.1 or more mole %, 1 or more mole%, 5 or more mole %, or 10 or more mole % of one or more modifyingglycols. Thus, if present, it is contemplated that the amount of one ormore modifying glycols can range from any of these preceding endpointvalues including, for example, from 0.01 to 15 mole % and from 0.1 to 10mole %.

Modifying glycols useful in the polyesters useful in the invention referto that are not listed as a required diol and may contain 2 to 16 carbonatoms. Examples of suitable modifying glycols include, but are notlimited to, diethylene glycol, ethylene glycol,2,2,4,4-tetramethyl-1,3-cyclobutanediol, 1,2-propanediol,1,3-propanediol, neopentyl glycol, 1,4-butanediol, 1,5-pentanediol,1,6-hexanediol, p-xylene glycol, isosorbide, or mixtures thereof. Inanother embodiment, the modifying glycols include but are not limited to1,3-propanediol and/or 1,4-butanediol. In another embodiment, at leastone modifying glycol is isosorbide. In one embodiment, suitablemodifying glycols include, but are not limited to, diethylene glycol,ethylene glycol, and 2,2,4,4-tetramethyl-1,3-cyclobutanediol. In oneembodiment, suitable modifying glycols include, but are not limited to,ethylene glycol, and 2,2,4,4-tetramethyl-1,3-cyclobutanediol. In oneembodiment, ethylene glycol is the modifying glycol. In one embodiment,2,2,4,4-tetramethyl-1,3-cyclobutanediol is the modifying glycol.

The polyesters useful in the invention can also comprise from 0 to 10mole percent, for example, from 0.01 to 5 mole percent, from 0.01 to 1mole percent, from 0.05 to 5 mole percent, from 0.05 to 1 mole percent,or from 0.1 to 0.7 mole percent, or 0.1 to 0.5 mole percent, based thetotal mole percentages of either the diol or diacid residues;respectively, of one or more residues of a branching monomer, alsoreferred to herein as a branching agent, having 3 or more carboxylsubstituents, hydroxyl substituents, or a combination thereof. Incertain embodiments, the branching monomer or agent may be added priorto and/or during and/or after the polymerization of the polyester. Thepolyester(s) useful in the invention can thus be linear or branched.

Examples of branching monomers include, but are not limited to,multifunctional acids or multifunctional alcohols such as trimelliticacid, trimellitic anhydride, pyromellitic dianhydride,trimethylolpropane, glycerol, pentaerythritol, citric acid, tartaricacid, 3-hydroxyglutaric acid and the like. In one embodiment, thebranching monomer residues can comprise 0.1 to 0.7 mole percent of oneor more residues chosen from at least one of the following: trimelliticanhydride, pyromellitic dianhydride, glycerol, sorbitol,1,2,6-hexanetriol, pentaerythritol, trimethylolethane, and/or trimesicacid. The branching monomer may be added to the polyester reactionmixture or blended with the polyester in the form of a concentrate asdescribed, for example, in U.S. Pat. Nos. 5,654,347 and 5,696,176, whosedisclosure regarding branching monomers is incorporated herein byreference.

The glass transition temperature (Tg) of the polyesters useful in theinvention was determined using a TA Instruments Q2000 DSC at a scan rateof 20° C./min.

In one embodiment, the polyesters of this invention can be visuallyclear. The term “visually clear” is defined herein as an appreciableabsence of cloudiness, haziness, and/or muddiness, when inspectedvisually. In another embodiment, when the polyesters are blended withanother polymer, the blends can be visually clear.

The polyesters useful in the invention can be made by processes knownfrom the literature such as, for example, by processes in homogenoussolution, by transesterification processes in the melt, and by two phaseinterfacial processes. Suitable methods include, but are not limited to,the steps of reacting one or more dicarboxylic acids with one or moreglycols at a temperature of 100° C. to 315° C. at a pressure of 0.1 to760 mm Hg for a time sufficient to form a polyester. See U.S. Pat. No.3,772,405 for methods of producing polyesters, the disclosure regardingsuch methods is hereby incorporated herein by reference.

In another aspect, the invention relates to a process for producing apolyester. The process comprises:

(I) heating a mixture comprising the monomers useful in any of thepolyesters useful in the invention in the presence of a catalyst at atemperature of 150 to 240° C. for a time sufficient to produce aninitial polyester;

(II) heating the initial polyester of step (I) at a temperature of 240to 320° C. for 1 to 4 hours; and

(III) removing any unreacted glycols.

Suitable catalysts for use in this process include, but are not limitedto, organo-zinc or tin compounds, including but not limited to, zincacetate, butyltin tris-2-ethylhexanoate, dibutyltin diacetate, and/ordibutyltin oxide. Other catalysts may include, but are not limited to,those based on titanium, zinc, manganese, lithium, germanium, andcobalt. A phosphorus compound may be used in connection with thisinvention. In one embodiment, the catalyst can be a combination ofmanganese, cobalt and germanium which can be used with phosphoruscompounds as described herein. In another embodiment, titanium andmanganese can be used. In one embodiment, tetrabutyl titanate can beused in combination with manganese acetate. In one embodiment, titaniumand tin catalysts can be combined. In one embodiment, tin can be used asthe only catalyst. In one embodiment, titanium can be used as the onlycatalyst. The invention further relates to a polyester product made bythe process described above.

The invention further relates to a polymer blend. The blend comprises:

(a) 0.01 to 99.99 weight % of at least one of the polyesters describedabove; and

(b) 0.01 to 99.995 weight % of at least one of the polymeric components.

Suitable examples of the polymeric components include, but are notlimited to, nylon, other polyesters different from those describedherien, nylon, polyamides such as ZYTEL® from DuPont; polyestersdifferent from those described herein; polystyrene, polystyrenecopolymers, styrene acrylonitrile copolymers, acrylonitrile butadienestyrene copolymers, poly(methylmethacrylate), acrylic copolymers,poly(ether-imides) such as ULTEM® (a poly(ether-imide) from GeneralElectric); polyphenylene oxides such as poly(2,6-dimethylphenyleneoxide) or poly(phenylene oxide)/polystyrene blends such as NORYL 1000®(a blend of poly(2,6-dimethylphenylene oxide) and polystyrene resinsfrom General Electric); other polyesters; polyphenylene sulfides;polyphenylene sulfide/sulfones; poly(ester-carbonates); polycarbonatessuch as LEXAN® (a polycarbonate from General Electric); polysulfones;polysulfone ethers; and poly(ether-ketones) of aromatic dihydroxycompounds or mixtures of any of the other foregoing polymers. The blendscan be prepared by conventional processing techniques known in the art,such as melt blending or solution blending.

The polyesters according to the invention can also be used in blends,such blends being obtainable by means of reactive extrusion too, withpolymers of natural origin, such as starch, cellulose, chitin andchitosan, alginates, proteins such as gluten, zein, casein, collagen,gelatine, natural rubbers, rosinic acid and its derivatives, lignins andtheir derivatives, natural fibers (such as for example jute, kenaf,hemp). The starches and celluloses may be modified and may include, forinstance, the starch and cellulose esters with a degree of substitutioncoming between 0.2 and 2.5, hydroxypropylated starches, and modifiedstarches with fatty chains. Starch can also be used in eitherdestructurized or gelatinised form, or as a filler. The starch mayrepresent the continuous or the dispersed phase, or it may be inco-continuous form. In the case of dispersed starch, the starchparticles can have mean dimension of less than 1μ, or less than 0.5μ.

With regard to the starch particles dimension, these are measured in thetransverse direction with respect to the direction of the extrusion flowor, anyhow, with respect to the direction of the material's output. Thedimension of a starch particle is therefore measured on thebidimensional shape resulting from the transverse direction. The meandimension is calculated as the numeral (or arithmetic) average of theparticle diameters.

In case of a spherical particle the particle diameter corresponds to thediameter of the smaller circle in which the particle can be inscribed.

In case of a non-spherical particle the particle diameter (d) iscalculated according to the following formula:d=√d₁d₂

where d₁ is the minor diameter and d₂ is the major diameter of theellipse in which the particle can be inscribed or approximated.

Mixtures of polyesters according to the invention wherein starchrepresents the dispersed phase can form biodegradable polymericcompositions with good-resistance to ageing and to humidity. Indeed,these polymeric compositions can maintain a high tear strength even incondition of low humidity.

Such characteristics can be achieved when the water content of thecomposition during mixing of the component is kept between 1% and 15% byweight. It is, however, also possible to operate with a content of lessthan 1% by weight, in this case, starting with predried andpre-plasticized starch.

It could be useful also to degrade starch at a low molecular weightbefore or during compounding with the polyesters of the presentinvention in order to have in the final material or finished product astarch inherent viscosity between 1 and 0.2 dl/g, or between 0.6 and0.25 dl/g, or between 0.55 and 0.3 dl/g.

Desctructurized starch can be obtained before or during mixing with thepolyesters according to the present invention in presence ofplasticizers such as water, glycerol, di and poly glycerols, ethylene orpropylene glycol, ethylene and propylene diglycol, polyethylene glycol,polypropylenglycol, 1,2 propandiol, trymethylol ethane, trymethylolpropane, pentaerytritol, dipentaerytritol, sorbitol, erytritol, xylitol,mannitol, sucrose, 1,3 propanediol, 1,2 butanediol, 1,3 butanediol, 1,4butanediol, 1,5 pentanediol, 1,5 hexanediol, 1,6 hexanediol, 1,2,6hexanetriol, 1,3,5 hexanetriol, neopentyl glycol and polyvinyl alcoholprepolymers and polymers, polyols acetates, ehtoxylates andpropoxylates, particularly sorbitol ethoxylate, sorbitol acetate, andpentaerythritol acetate. The quantity of high boiling point plasticizers(plasticizers different from water) used are generally from 0% to 50%,or from 10% to 30% by weight, relative to the starch.

Water can be used as a plasticizer in combination with high boilingpoint plasticizers or alone during the plastification phase of starchbefore or during the mixing of the composition and can be removed at theneeded level by degassing on one or more steps during extrusion. Uponcompletion of the plastification and mixing of the components, the wateris removed by degassing to give a final content of about 0.2-3% byweight.

Water, as well as high-boiling point plasticizers, modifies theviscosity of the starch phase and affects the rheological properties ofthe starch/polymer system, helping to determine the dimensions of thedispersed particles. Compatibilizers can be also added to the mixture.They can belong to the following classes:

Additives such as esters which have hydrophilic/lipophilic balance indexvalues (HLB) greater than 8 and which are obtained from polyols and frommono or polycarboxylic acids with dissociation constants pK lower than4,5 (the value relates to pK of the first carboxyl group in the case ofpolycarboxylic acids);

Esters with HLB values of between 5,5 and 8, obtained from polyols andfrom mono or polycarboxylic acids with less than 12 carbon atoms andwith pK values greater than 4.5 (this value relates to the pK of thefirst carboxylic group in the case of polycarboxylic acids);

Esters with HLB values lower than 5.5 obtained from polyols and fromfatty acids with 12-22 carbon atoms.

These compatibilizers can be used in quantities of from 0.2 to 40%weight and or from 1 to 20% by weight related to the starch. The starchblends can also contain polymeric compatibilizing agents having twocomponents: one compatible or soluble with starch and a second onesoluble or compatible with the polyester.

Examples are starch/polyester copolymers through transesterificationcatalysts. Such polymers can be generated through reactive blendingduring compounding or can be produced in a separate process and thenadded during extrusion, In general block copolymers of an hydrophilicand an hydrophobic units are particularly suitable. Additives such as diand polyepoxides, di and poly isocyanates, isocyanurates,polycarbodiimmides and peroxides can also be added. They can work asstabilizers as well as chain extenders.

All the products above can help to create the needed microstructure.

The starch/polyester ratio can be comprised in the range 5/95% weight upto 60/40% by weight, or 10/90-45/55% by weight.

In such starch-based blends in combination with the polyesters of thepresent invention it is possible to add polyolefins, polyvinyl alcoholat high and low hydrolysis degree, ethylene vinylalcohol and ethylenevinylacetate copolymers and their combinations as well as aliphaticpolyesters such as polybuthylenesuccinate, polybuthylenesuccinateadipate, polybuthylensuccinate adipate-caprolactate,polybuthylensuccinate-lactate, polycaprolactone polymers and copolymers,PBT, PET, PTT, polyamides, polybuthylen terephthalate adipates with acontent of terephthalic acid between 40 and 70% with and withoutsulfonated groups with or without branches and possibly chain extendedwith diisocyanates or isocyanurates, polyurethanes, polyamide-urethanes,cellulose and starch esters such as acetate, propionate and butryatewith substitution degrees between 1 and 3, or between 1.5 and 2.5,polyhydroxyalkanoates, poly L-lactic acid, poly-D lactic acid andlactides, their mixtures and copolymers.

The starch blends of the polyesters of the present invention can beeasily processable in film blowing even at MFI (170° C., 5 kg) of 7 g/10min. Moreover, they can have impact strength higher than 20 kJ/m², orhigher than 30 kJ/m²′ or higher than 45 kJ/m² (measured on blown film 30μm thick at 10° C. and less than 5% relative humidity). Particularlyresistant and easily processable compounds contain destructurized starchin combination with the polyesters of the invention and polylactic acidpolymers and copolymers with and without additives such as polyepoxides,carbodiimmides and/or peroxides.

The starch-base films can be even transparent in case of nanoparticlesof starch with dimensions lower than 500 μm or lower than 300 μm. It isalso possible to go from a dispersion of starch in form of droplets to adispersion in which two co-continuous phases coexist and the blend ischaracterized for allowing a higher water content during processing.

In general, to obtain co-continuous structures it is possible to workeither on the selection of starch with high amylopectine content and/orto add to the starch-polyester compositions block copolymers withhydrophobic and hydrophilic units. Possible examples arepolyvinylacetate/polyvinylalcohol and polyester/polyether copolymers inwhich the block length, the balance between the hydrophilicity andhydrophobicity of the blocks and the quality of compatibilizer used canbe suitably changed in order to finely adjust the microstructure of thestarch-polyester compositions.

The polymers according to the invention can also be blended withpolyolefins, such as polyethylene, polypropylene and their copolymers,polyvinyl alcohol, polyvinyl acetate, polyethyl vinyl acetate andpolyethylene vinyl alcohol, polyester urethanes, polyurethanes,polyamides, polyureas and aromatic polyesters of the diacid diol typewherein the aromatic acid is 2.5 furandicarboxylic acid.

The polymers according to the invention can also be used as prepolymersin the production of polyurethanes and polyureas.

In one embodiment, the polyesters of the invention are blended withstarch.

The polyesters according to the invention can also be used in blendswith polymers of synthetic origin and with the previously-mentionedpolymers of natural origin.

Binary and ternary blends of the polyester according to the presentinvention with biodegradable polyesters of the type disclosed aboveand/or with polymers of natural origin are particularly suitable for theproduction of films. Advantageously, the films obtained with said blendsshow excellent mechanical properties.

In one embodiments, the polyesters of the invention can be mixed withstarch and polylactic acid.

Blends of the polyesters according the present invention with PLA are ofparticular interest because their high compatibility with PLA polymersand copolymers permits to cover materials with a wide range ofrigidities—which makes these blends particularly suitable for injectionmolding and extrusion.

Moreover, blends of such polyesters with poly L-lactic acid and polyD-lactic acid or poly L-lactide and D-lactide where the ratio betweenpoly L- and poly D-lactic acid or lactide is in the range 10/90-90/10,or 20/80-80/20, and the ratio between aliphatic-aromatic polyester andthe polylactic acid or PLA blend is in the range 5/95-95/5, or10/90-90/10, are of particular interest for the high thermal resistance.Polylactic acid or lactide polymers or copolymers are generally ofmolecular weight Mn in the range between 30,000 and 30,000 or between50,000 and 250,000.

To improve the transparency and toughness of such blends and decrease oravoid a lamellar structure of polylactide polymers, it is possible tointroduce other polymers as compatibilizers or toughening agents suchas: polybutylene succinate and copolymers with adipic acid and or lacticacid and or hydroxyl caproic acid, polycaprolactone, aliphatic polymersof diols from C2 to C13 and diacids from C4 to C13,polyhydroxyalkanoates, polyvinylalcohol in the range of hydrolysisdegree between 75 and 99% and its copolymers, polyvinylacetate in arange of hydrolysis degree between 0 and 70%, or between 0 and 60%. Inone embodiment, the diols used in the polyesters of the invention can bechosen from ethylene glycol, propandiol, butanediol and the acids usedin the polyesters of the invention can be chosen from: azelaic, sebacic,undecandioic acid, dodecandioic acid, brassylic acid and theircombinations.

To maximize compatibility among the polyesters of the invention andpolylactic acid it is very useful the introduction of copolymers withblocks having high affinity for the aliphatic-aromatic copolyesters ofthe invention, and blocks with affinity for the lactic acid polymers orcopolymers. One embodiment of the invention can be block copolymers ofthe aliphatic aromatic copolymers of the invention with polylactic acid.Such block copolymers can be obtained taking the two original polymersterminated with hydroxyl groups and then reacting such polymers withchain extenders able to react with hydroxyl groups such asdiisocyanates.

Examples are 1,6 hexamethylene diisocyanate, isophorone diisocyanate,methylene diphenildiisocyanate, toluene diisocyanate or the like. It isalso possible to use chain extenders able to react with carboxylicgroups like di and poly epoxides (e.g. bisphenols diglycidyl ethers,glycerol diglycidyl ethers) divinyl derivatives if the polymers of theblend are terminated with acid groups. It is possible also to use aschain extenders carbodiimmides, bis-oxazolines, isocyanurates etc.

The intrinsic viscosity of such block copolymers can be between 0.3 andl=1.5 dl/g, or between 0.45 and 1.2 dl/g. The amount of compatibilizerin the blend of aliphaticaromatic copolyesters and polylactic acid canbe in the range between 0.5 and 50% by weight, or between 1 and 30% byweight, or between 2 and 20% by weight.

The polyesters according to the present invention can advantageously beblended also with nucleating agents and filler both of organic andinorganic nature.

Examples of nucleating agents include talc, saccharine sodium salt,calcium silicate, sodium benzoate, calcium titanate, boron nitride, zincsalts, porphyrin, chlorine, phlorin, porphodimethine, porphomethine,bacteriochlorin, isobacteriochorin, porphyrinogen, phorbin, isotacticpolypropylene, PLA with low molecular weight and PBT.

In one embodiment, the amount of fillers can be in the range of 0.5-70%by weight, or 5-50% by weight.

As regards organic fillers, wood powder, proteins, cellulose powder,grape residue, bran, maize husks, compost, other natural fibres, cerealgrits with and without plasticizers such as polyols can be mentioned.

As regards inorganic fillers, it can be mentioned substances that areable to be dispersed and/or to be reduced in lamellas with submicronicdimensions, for example, less than 500 ntn or less than 300 nm, or lessthan 50 nm. In one embodiment, inorganic fillers can be selected fromzeolites and silicates of various kind such as wollastonites,montmorillonites, hydrotalcites also funetionalised with molecules ableto interact with starch and or the specific polyester. The use of suchfillers can improve stiffness, water and gas permeability, dimensionalstability and maintain transparency.

The biodegradable polyesters according to the invention arebiodegradable according to the standard EN 13432.

The process for producing the polyesters according to the presentinvention can be conducted using any of the known processes according tothe state of the art. In particular, the polyesters can beadvantageously obtained using a polycondensation reaction. Thecopolyester polymerisation process can be advantageously conducted inthe presence of a suitable catalyst. An example of a suitable catalystmight be the organometallc compounds of tin such as the derivatives ofstannoic acid, or the compounds of titanium such as orthobutyl titanate,or the compounds of aluminium such as Al-triisopropyl, or of antimonyand zinc.

In addition, the polyester compositions and the polymer blendcompositions containing the polyesters useful in this invention may alsocontain from 0.01 to 25% by weight or 0.01 to 20% by weight or 0.01 to15% by weight or 0.01 to 10% by weight or 0.01 to 5% by weight of thetotal weight of the polyester composition of common additives such ascolorants, dyes, mold release agents, release agents that release thepolymer from rolls of the manufacturing equipment, flame retardants,plasticizers, nucleating agents, stabilizers, including but not limitedto, UV stabilizers, thermal stabilizers and/or reaction productsthereof, fillers, and impact modifiers. Examples of typical commerciallyavailable impact modifiers well known in the art and useful in thisinvention include, but are not limited to, ethylene/propyleneterpolymers; functionalized polyolefins, such as those containing methylacrylate and/or glycidyl methacrylate; styrene-based block copolymericimpact modifiers; and various acrylic core/shell type impact modifiers.For example, UV additives can be incorporated into articles ofmanufacture through addition to the bulk, through application of a hardcoat, or through coextrusion of a cap layer. Residues of such additivesare also contemplated as part of the polyester composition.

In the case of adding release agents which reduce adhesion tomanufacturing equipment such as calendering rolls, these can be selectedfrom the group comprising esters of fatty acids and amides, and metalsalts, soaps, paraffin, or hydrocarbon waxes such as: zinc stearate,calcium stearate, aluminum stearate, stearamides, erucamides,behenamides, white beeswax, candelilla wax, LDPE with high MFI such asEastman Epolene N21, Epolene E20, and Lofio HOB 7119.

An increase in the molecular weight of the polyesters can beadvantageously obtained, for instance, by adding various organicperoxides during the extrusion process. The increase in the molecularweight of the biodegradable polyesters is easily detectable on observingthe increase in the viscosity values after processing the polyesterswith the peroxides.

Examples of peroxides that can advantageously be used are selected fromthe group of dialkyl peroxides, such as: benzoyl peroxide, lauroylperoxide, isononanoyl peroxide, di-(tbutylperoxyisopropyl)benzene,t-butyl peroxide, dicumyl peroxide, alpha,alpha-di(t-20butylperoxy)diisopropylbenzene, 2,5-dimethyl-2,5di(t-butylperoxy)hexane, t-butyl cumyl peroxide, di-t-butylperoxide,2,5-dimethyl-2,5-di(t-butylperoxy)hex-3-yne,di(4-tbutylcyclohexyl)peroxydi-carbonate, dicetyl peroxydicarbonate,dimyristyl peroxydicarbonate,3,69-triethyl-3,6,9-trimethyl-1,4,7-triperoxonan,di(2-ethylhexyl)peroxydicarbonate and mixtures thereof.

In one embodiment, peroxides can be added to the polyesters according tothe invention in a quantity of less than 0.5% by weight, or less than0.01-0.2% by weight, or less than 0.01-0.1% by weight.

The polyesters of the invention can comprise at least one chainextender. Suitable chain extenders include, but are not limited to,multifunctional (including, but not limited to, bifunctional)isocyanates, multifunctional epoxides, including for example, epoxylatednovolacs, and phenoxy resins. In certain embodiments, chain extendersmay be added at the end of the polymerization process or after thepolymerization process. If added after the polymerization process, chainextenders can be incorporated by compounding or by addition duringconversion processes such as injection molding or extrusion. The amountof chain extender used can vary depending on the specific monomercomposition used and the physical properties desired but can be selectedfrom 0.1 percent by weight to about 10 percent by weight, or from 0.1 toabout 5 percent by weight, based on the total weight of the polyester.

The polyesters of the invention can contain phosphorous compoundsincluding but not limited to phosphoric acid, phosphorous acid,phosphonic acid, phosphinic acid, phosphonous acid, and various estersand salts thereof. These can be present in the polyester compositionsuseful in the invention. The esters can be alkyl, branched alkyl,substituted alkyl, difunctional alkyl, alkyl ethers, aryl, andsubstituted aryl. In one embodiment, the number of ester groups presentin the particular phosphorous compound can vary from zero up to themaximum allowable based on the number of hydroxyl groups present on thephosphorus compound used. Examples of phosphorus compounds useful in theinvention can include phosphites, phosphates, phosphinates, orphosphonites, including the esters thereof.

The polyesters of the invention can have good molecular weight. In oneembodiment, the number average molecular weight of the polyesters is atleast 10,000. In one embodiment, the number average molecular weight ofthe polyesters is at least 20,000.

Reinforcing materials may be useful in the compositions of thisinvention. The reinforcing materials may include, but are not limitedto, carbon filaments, silicates, mica, clay, talc, titanium dioxide,Wollastonite, glass flakes, glass beads and fibers, and polymeric fibersand combinations thereof. In one embodiment, the reinforcing materialsare glass, such as, fibrous glass filaments, mixtures of glass and talc,glass and mica, and glass and polymeric fibers.

In another embodiment, the invention further relates to articles ofmanufacture comprising any of the polyesters and blends describedherein.

The present polyesters and/or polyester blend compositions can be usefulin forming fibers, films, molded articles, foamed articles, containers,bottles and sheeting. The methods of forming the polyesters into fibers,films, molded articles, containers, and sheeting are well known in theart.

The invention further relates to articles of manufacture. These articlesinclude, but are not limited to, injection molded articles, injectionblow molded articles, injection stretch blow molded articles, extrusionblow molded articles, extrusion stretch blow molded articles, extrusioncoatings, calendered articles, compression molded articles, and solutioncasted articles. Methods of making the articles of manufacuture,include, but are not limited to, extrusion blow molding, extrusionstretch blow molding, injection blow molding, injection stretch blowmolding, calendering, rotomolding, compression molding, and solutioncasting.

The polyesters according to the invention have properties and viscosityvalues that make them suitable, after adjusting their molecular weight,for use in numerous practical applications such as films, injectionmolded products, extrusion coatings, fibres, foams, thermoformedproducts, extruded profiles and sheets, extrusion blow molding,injection blow molding, rotomolding, stretch blow molding, etc.

In another embodiment, the invention further relates to articles ofmanufacture comprising the film(s) and/or sheet(s) containing polyestercompositions described herein. In another embodiment, the inventionrelates to fibers. In yet another embodiment, the invention relates tofoams. In another embodiment, this invention relates to thermoformedarticles. In another embodiment, this invention relates to packagingmaterials.

The methods of forming polyesters into film(s) and/or sheet(s) are wellknown in the art. Examples of film production technologies include filmblowing, casting and coestrusion. Examples of film(s) and/or sheet(s) ofthe invention including but not limited to extruded film(s) and/orsheet(s), calendered film(s) and/or sheet(s), compression molded film(s)and/or sheet(s), solution casted film(s) and/or sheet(s). Methods ofmaking film and/or sheet include but are not limited to extrusion,calendering, compression molding, and solution casting.

Examples of potential articles made from film and/or sheet include, butare not limited, to uniaxially stretched film, biaxially stretched film,shrink film (whether or not uniaxially or biaxially stretched), liquidcrystal display film (including, but not limited to, diffuser sheets,compensation films and protective films), thermoformed sheet, graphicarts film, outdoor signs, skylights, coating(s), coated articles,painted articles, laminates, laminated articles, and/or multiwall filmsor sheets.

Films obtained, with the polyester according to the present inventionshow excellent mechanical properties, such as for example an ultimateelongation greater than 350%, or greater than 400%, or greater than 500%with an ultimate energy greater than 70 MJ/m³, or greater than 90 MJ/m³or greater than 100 MJ/m³.

Moreover, such films can be subject to biorientation in line or afterfilm production. The films can be also oriented through stretching inone direction with a stretching ratio from 1:2 up to 1:15, or from 1:2.2up to 1:8. It is also possible that the stretching is obtained inpresence of an highly filled material with inorganic fillers. In such acase, the stretching can generate microholes and the so obtained filmcan be particularly suitable for hygiene applications.

In particular, the polyesters according to the invention are suitablefor manufacturing:

mono- and bi-oriented films, and films multilayered with other polymers;

films for use in the agricultural sector, such as films for use inmulching;

cling films for use with foodstuffs, for bales in agriculture, and forwrapping waste;

shrink film such as for example for pallets, mineral water, six packrings, and so on;

bags and bin liners for the organic waste collection, e.g. thecollection of food scraps and gardening waste;

thermoformed foodstuff packaging, both mono- and multi-layered, as incontainers for milk, yogurt, meats, beverages, etc;

coatings obtained, using the extrusion coating method; multilayerlaminates with rigid or flexible backings such as for example paper,plastic, aluminium, or metallic films;

foamed or foamable beads for the production of pieces obtained bysintering;

foamed and semi-foamed products, including foamed blocks formed usingpre-expanded articles;

foamed sheets, thermoformed foam sheets, and containers obtained fromthem for use in foodstuff packaging;

fruit and vegetable containers in general; composites with gelatinised,destructured and/or complexed starch, natural starch, flours, otherfillers of natural, vegetal or inorganic origin;

fibres, microfibres, composite fibres with a core consisting of rigidpolymers, such as PLA, PET, PTT etc., and an external shell made usingthe material according to the invention, dablens composite fibres,fibres with different cross sections, from round to multilobed, fibresin flakes, woven and nonwoven, or spun-bonded or thermobonded fabricsfor use in sanitary and hygiene products, and in the agricultural andclothing sectors.

Other uses may also include applications in which the polyesters areused in lieu of plastic coated PVC.

As used herein, the abbreviation “wt” means “weight”.

The following examples further illustrate how the compositions of matterof the invention can be made and evaluated, and are intended to bepurely exemplary of the invention and are not intended to limit thescope thereof. Unless indicated otherwise, parts are parts by weight,temperature is in degrees C. or is at room temperature, and pressure isat or near atmospheric.

EXAMPLES

Unless otherwise specified, the cis/trans ratio of the 1,4cyclohexanedimethanol used in the following examples was approximately30/70, and could range from 35/65 to 25/75.

The following abbreviations apply throughout the working examples andfigures:

TPA Terephthalic acid DMT Dimethyl terephthalate CHDM1,4-cyclohexanedimethanol TMCD 2,2,4,4-tetramethyl-1,3-cyclobutanediolFDCA 2,5-Furandicarboxylic Acid IhV or IV Inherent Viscosity T_(g) Glasstransition temperature EG Ethylene Glycol

All polymers in the examples were prepared by standard melt-phasepolycondensation polymerization techniques known in the art. The polymerinherent viscosity (IhV) was measured by solution viscometry, usingPhenol/1,1,2,2-tetrachloroethane (60/40) as a solvent. The polymer glasstransition temperatures were measured by differential scanningcalorimetry (DSC) with a TA Q2000 Differential Scanning calorimeter withrefrigerated cooling accessory (RCA), with the first heating from 0 to280° C. at 20° C./min, followed by cooling to 0° C. at 20° C./min, andheating again (second heating) from 0 to 280° C. at 20° C./min. Theglass transition temperature (Tg) was recorded during the second heatingcycle. Polymer compositions (mole percent glycols) were measured byproton nuclear magnetic resonance spectroscopy (NMR) using standardmethods known in the art.

TABLE 1 Summary of Examples and Comparative Examples Mole % Mole % Mole% Mole % Mole % IhV, Tg, Example TPA FDCA EG CHDM TMCD dL/g ° C. Example1 (PCF) 0 100 0 100 0 0.81 86 Example 2 0 100 0 73 27 0.70 96 Example 3100 0 0 72 28 0.70 114 Example 4 (PEFG) 0 100 69 31 0 0.76 84 Example 5(PCFG) 0 100 41 59 0 0.90 85 Example 6 (PET) 100 0 100 0 0 1.00 80Example 7 (PETG) 100 0 69 31 0 1.07 83 Example 8 (PCTG) 100 0 38 62 00.98 89 Example 9 (PCT) 100 0 0 100 0 0.85 95 Example 10 (PEF) 0 100 1000 0 0.72 87

Example 1 Poly(1,4-cyclohexylenedimethylene furandicarboxylate), PCF

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.1 mole FDCA (15.7 g), 0.11 mole CHDM(15.1 g), and a solution of titanium tetraisopropoxide in ethyleneglycol such that the concentration of Ti was approximately 50 ppm basedupon final polymer weight. The mixture was heated to 200° C. whilestirring at atmospheric pressure under a N2 purge until a well-dispersedslurry was obtained. The temperature was then increased to 285° C. overa period of about 15 minutes, at which point a clear liquid melt wasobserved. The pressure was then slowly reduced to 0.5 Torr by means of avacuum pump and held for about 60 minutes, collecting condensate in asidearm flask cooled with dry ice located between the reaction flask andthe vacuum pump. The resulting polymer was cooled to room temperature,separated from the flask, and cryogenically ground. The resultingpolymer had IhV=0.81 dL/g and Tg=86° C.

Example 2 Poly(cyclohexylmethylene-tetramethylcyclobutylene furanoate)

A 500 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.15 mole DMF (27.6 g), 0.11 mole CHDM(15.6 g), 0.05 mole (7.3 g) 2,2,4,4-tetramethyl-1,3-cyclobutanediol anda solution of tin (IV) catalyst such that the concentration of tin wasapproximately 200 ppm based upon final polymer weight. The mixture washeated to 200° C. for while stirring at atmospheric pressure under a N2purge. The temperature was then slowly increased to 265° C. over aperiod of about one hour. The pressure was then slowly reduced to about0.3 Torr by means of a vacuum pump and held for about 30 minutes,collecting condensate in a sidarm flask cooled with dry ice locatedbetween the reaction flask and the vacuum pump. The resulting polymerwas cooled to room temperature, separated from the flask, andcryogenically ground. The resulting polymer had glycol composition 27mole % TMCD and 73 mole % CHDM. The resulting polymer had IhV=0.70 dL/gand Tg=96° C.

Example 3 Poly(cyclohexylmethylene-tetramethylcyclobutyleneterephthalate)

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.15 mole DMT (29.1 g), 0.11 mole CHDM(15.6 g), 0.05 mole TMCD (7.1 g) and a solution of tin (IV) catalystsuch that the concentration of tin was approximately 200 ppm based uponfinal polymer weight. The mixture was heated to 200° C. for whilestirring at atmospheric pressure under a N2 purge. The temperature wasthen slowly increased to 265° C. over a period of about one hour. Thepressure was then slowly reduced to about 0.3 Torr by means of a vacuumpump and held for about 30 minutes, collecting condensate in a sidarmflask cooled with dry ice located between the reaction flask and thevacuum pump. The resulting polymer was cooled to room temperature,separated from the flask, and cryogenically ground. The resultingpolymer had glycol composition 28 mole & TMCD and 72 mole % CHDM. Theresulting polymer had IhV=0.70 dL/g and Tg=114° C.

Example 4 Glycol-modified poly(ethylene furandicarboxylate), PEFG

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.12 mole FDCA (18.7 g), 0.04 moleCHDM (5.6 g), 0.20 mole EG (12.5 g) and a solution of titaniumtetraisopropoxide in ethylene glycol such that the concentration of Tiwas approximately 50 ppm based upon final polymer weight. The mixturewas heated to 200° C. for about 80 minutes while stirring at atmosphericpressure under a N2 purge. The pressure was then slowly reduced to 130Torr by means of a vacuum pump and the temperature increased to 245° C.and held for about 30 minutes, collecting condensate in a sidearm flaskcooled with dry ice located between the reaction flask and the vacuumpump. The pressure was then slowly reduced to 0.5 Torr and thetemperature increased to 260° C. and held for about one hour. Theresulting polymer was cooled to room temperature, separated from theflask, and cryogenically ground. The resulting polymer had a glycolconstituent composition of about 31 mole percent CHDM. The resultingpolymer had IhV=0.76 dL/g and Tg=84° C.

Example 5 Glycol-modified poly(1,4-cyclohexylenedimethylenefurandicarboxylate), PCFG

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.12 mole FDCA (18.7 g), 0.07 moleCHDM (10.7 g), 0.17 mole EG (10.3 g) and a solution of titaniumtetraisopropoxide in ethylene glycol such that the concentration of Tiwas approximately 50 ppm based upon final polymer weight. The mixturewas heated to 200° C. for about 60 minutes while stirring at atmosphericpressure under a N2 purge. The pressure was then slowly reduced to 130Torr by means of a vacuum pump and the temperature increased to 245° C.and held for about 30 minutes, collecting condensate in a sidearm flaskcooled with dry ice located between the reaction flask and the vacuumpump. The pressure was then slowly reduced to 0.5 Torr and thetemperature increased to 260° C. and held for about 80 minutes. Theresulting polymer was cooled to room temperature, separated from theflask, and cryogenically ground. The resulting polymer had a glycolconstituent composition of about 59 mole percent CHDM. The resultingpolymer had IhV=0.90 dL/g and Tg=85° C.

Example 6 Poly(ethylene terephthalate), PET

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.1 mole terephthalic acid, TPA, (16.6g), 0.30 mole EG (18.6 g), and a solution of titanium tetraisopropoxidein ethylene glycol such that the concentration of Ti was approximately500 ppm based upon final polymer weight. The mixture was heated to 185°C. for about 14 hours while stirring at atmospheric pressure under a N2purge. The temperature was then increased to 230° C. for about 30minutes. The temperature was then increased to about 245° C. for about30 minutes, at which point a clear liquid melt was observed. Thepressure was then slowly reduced to 130 Torr by means of a vacuum pumpand the temperature increased to 260° C. and held for about 30 minutes,collecting condensate in a sidearm flask cooled with dry ice locatedbetween the reaction flask and the vacuum pump. The pressure was thenslowly reduced to 0.5 Torr and the temperature increased to 275° C. andheld for about 45 minutes. The resulting polymer was cooled to roomtemperature, separated from the flask, and cryogenically ground. Theresulting polymer had IhV=1.00 dL/g and Tg=80° C.

Example 7 Glycol-modified poly(ethylene terephthalate), PETG

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.12 mole terephthalic acid, TPA,(19.9 g), 0.04 mole CHDM (5.3 g), 0.20 mole EG (12.6 g), and a solutionof titanium tetraisopropoxide in ethylene glycol such that theconcentration of Ti was approximately 25 ppm based upon final polymerweight. The mixture was heated to 185° C. for about 17 hours whilestirring at atmospheric pressure under a N2 purge. The temperature wasthen increased to 230° C. for about 60 minutes. The temperature was thenincreased to about 245° C. for about 60 minutes, at which point a clearliquid melt was observed. The pressure was then slowly reduced to 130Torr by means of a vacuum pump and the temperature increased to 260° C.and held for about 60 minutes, collecting condensate in a sidearm flaskcooled with dry ice located between the reaction flask and the vacuumpump. The pressure was then slowly reduced to 4 Torr and the temperatureincreased to 270° C. and held for about 30 minutes. The pressure wasthen slowly reduced to 0.5 Torr and held for about 90 minutes. Theresulting polymer was cooled to room temperature, separated from theflask, and cryogenically ground. The resulting polymer had a glycolconstituent composition of about 30 mole percent CHDM. The resultingpolymer had IhV=1.07 dL/g and Tg=83° C.

Example 8 Glycol-modified poly(1,4-cyclohexylenedimethyleneterephthalate), PCTG

A 100 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.05 mole TPA, (8.3 g), 0.05 moledimethyl terephthalate (DMT, 9.7 g), 0.07 mole CHDM (9.5 g), 0.13 moleEG (8.3 g), and a solution of titanium tetraisopropoxide in ethyleneglycol such that the concentration of Ti was approximately 50 ppm basedupon final polymer weight. The mixture was heated to 200° C. for about60 minutes while stirring at atmospheric pressure under a N2 purge. Thetemperature was then increased to 210° C. and held for about 60 minutes.The temperature was then increased to 245° C. and held for about 45minutes. The pressure was then slowly reduced to 130 Torr by means of avacuum pump and the temperature increased to 260° C. and held for about30 minutes, collecting condensate in a sidearm flask cooled with dry icelocated between the reaction flask and the vacuum pump. The pressure wasthen slowly reduced to 4 Torr and the temperature increased to 275° C.and held for about 15 minutes. The pressure was then slowly reduced to0.5 Torr and held for about 45 minutes. The resulting polymer was cooledto room temperature, separated from the flask, and cryogenically ground.The resulting polymer had a glycol constituent composition of about 62mole percent CHDM. The resulting polymer had IhV=0.98 dL/g and Tg=89° C.

Example 9 Poly(1,4-cyclohexylenedimethylene terephthalate), PCT

A 500 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.5 mole dimethyl terephthalate (DMT,97.0 g), 0.55 mole CHDM (79.2 g) and a solution of titaniumtetraisopropoxide in ethylene glycol such that the concentration of Tiwas approximately 100 ppm based upon final polymer weight. The mixturewas heated to 220° C. while stirring at atmospheric pressure under a N2purge until a clear melt was obtained. The temperature was thenincreased to 290° C. over a period of about 30 minutes. The pressure wasthen slowly reduced to about 0.3 Torr by means of a vacuum pump and heldfor about 50 minutes, collecting condensate in a sidarm flask cooledwith dry ice located between the reaction flask and the vacuum pump. Theresulting polymer was cooled to room temperature, separated from theflask, and cryogenically ground. The resulting polymer had IhV=0.85 dL/gand Tg=95° C.

Example 10 Poly(ethylene furandicarboxylate), PEF

A 500 ml round-bottom flask fitted with a sidearm and condensatecollection flask was charged with 0.5 mole FDCA (78.0 g), 1 mole EG(62.1 g), and a solution of titanium tetraisopropoxide in ethyleneglycol such that the concentration of Ti was approximately 50 ppm basedupon final polymer weight. The mixture was heated to 200° C. for aboutone hour while stirring at atmospheric pressure under a N2 purge. Thetemperature was then increased to 215° C. for about one hour. Thepressure was then slowly reduced to about 0.3 Torr by means of a vacuumpump, and the temperature increased to 260° C. and held for about one totwo hours, collecting condensate in a sidarm flask cooled with dry icelocated between the reaction flask and the vacuum pump. The resultingpolymer was cooled to room temperature, separated from the flask, andcryogenically ground. The resulting polymer had IhV=0.72 dL/g and Tg=87°C.

It can be clearly seen from a comparison of the data in the aboverelevant working examples that the polyesters of the present inventionoffer a definite advantage over the commercially available polyesters.

The invention has been described in detail with reference to theembodiments disclosed herein, but it will be understood that variationsand modifications can be effected within the spirit and scope of theinvention.

We claim:
 1. A polyester composition comprising at least one polyesterformed from solely one dicarboxylic component and solely one glycolcomponent, (a) said dicarboxylic acid component comprising: i) 70 to 100mole % of 2,5-furandicarboxylic acid residues; ii) 0 mole % of aromaticdicarboxylic acid residues having up to 20 carbon atoms; and iii) 0 to30 mole % of aliphatic dicarboxylic acid residues having up to 16 carbonatoms; and (b) said glycol component comprising: i) 1 to 99 mole % of1,4-cyclohexanedimethanol (CHDM) residues; and ii) 1 to 99 mole % ofresidues of a modifying glycol selected from the group consisting ofdiethylene glycol, ethylene glycol,2,2,4,4-tetramethyl-1,3-cyclobutanediol, 1,2-propanediol,1,3-propanediol, neopentyl glycol, 1,4-butanediol, 1,5-pentanediol,1,6-hexanediol, p-xylene glycol, and mixtures thereof, wherein the totalmole % of the dicarboxylic acid component is 100 mole %, and the totalmole % of the glycol component is 100 mole %, and wherein the sum of theresidues of CHDM and the modifying glycol is equal to 100 mole % of theglycol component.
 2. The polyester composition of claim 1, wherein theinherent viscosity is from 0.35 to less than 1.0 dL/g.
 3. The polyestercomposition of claim 1, wherein the inherent viscosity is from 0.35 to0.80 dL/g.
 4. The polyester composition of claim 1, wherein the inherentviscosity is from 0.50 to 0.75 dL/g.
 5. The polyester composition ofclaim 1, wherein the glycol component comprises 15 to 80 mole % of1,4-cyclohexanedimethanol residues.
 6. The polyester composition ofclaim 1, wherein the glycol component comprises 25 to 50 mole % of1,4-cyclohexanedimethanol residues.
 7. The polyester composition ofclaim 1, wherein the glycol component of said polyester comprises 50 to70 mole % of 1,4-cyclohexanedimethanol residues.
 8. The polyestercomposition of claim 1, wherein the glycol component of said polyestercomprises 5 to less than 50 mole % of2,2,4,4-tetramethyl-1,3-cyclobutanediol residues and greater than 50 to95 mole % of 1,4-cyclohexanedimethanol residues.
 9. The polyestercomposition of claim 1, wherein the glycol component of said polyestercomprises 10 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues and 70 to 90 mole % of 1,4-cyclohexanedimethanol residues. 10.The polyester composition of claim 1, wherein the glycol componentcomprises 30 to 40 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediolresidues and 60 to 70 mole % of 1,4-cyclohexanedimethanol residues. 11.The polyester composition of claim 1, wherein the glycol componentcomprises 25 to 50 mole % of 1,4-cyclohexanedimethanol residues and 50to 75 mole % of ethylene glycol residues.
 12. The polyester compositionof claim 1, wherein the glycol component of said polyester comprises 50to 70 mole % of 1,4-cyclohexanedimethanol residues and 30 to 50 mole %of ethylene glycol residues.
 13. The polyester composition of claim 1,wherein the dicarboxylic acid component comprises 80 to 100 mole % of2,5-furandicarboxylic acid residues.
 14. The polyester composition ofclaim 1, wherein the dicarboxylic acid component comprises 90 to 100mole % of 2,5-furandicarboxylic acid residues.
 15. The polyestercomposition of claim 1, wherein said polyester composition comprises atleast one polymer chosen from poly(etherimides), polyphenylene oxides,poly(phenylene oxide)/polystyrene blends, polystyrene resins,polyphenylene sulfides, polyphenylene sulfide/sulfones,poly(ester-carbonates), polycarbonates, polysulfones, polysulfoneethers, starches, cellulose esters, and poly(ether-ketones).
 16. Thepolyester composition of claim 1, wherein said polyester comprisesresidues of at least one branching agent in an amount of 0.01 to 10 mole% based on the total mole percentage of the diacid or diol residues. 17.An article of manufacture comprising the polyester composition ofclaim
 1. 18. An article of manufacture selected from film, fiber, sheet,bottle, foam, foamed article, thermoformed article or a coatingaccording to claim
 17. 19. The polyester composition of claim 1, whereinthe polyester has a Tg in the range of 80 to 100° C. as the amount ofCHDM residues is increased from 1 to 99 mole %.
 20. The polyestercomposition of claim 1, wherein the polyester has a Tg in the range of80 to 90° C. as the amount of CHDM residues is increased from 1 to 99mole %.